The objective is to investigate the treatment of non-anemic iron deficiency (NAID) and the impact on development of anemia later in pregnancy. Anemia in the third trimester has been identified as a risk factor for maternal and fetal morbidity that might lead to mortality. Due to the high incidence of NAID in pregnancy, there is an opportunity for early screening and treatment to decrease progression to anemia. The primary aim of this study is to establish if treatment of NAID will result in higher third trimester hemoglobin values and decrease incidence of anemia at term.

Start Date12 Aug 2022

Sponsor / Collaborator

Stony Brook University

NCT04930237 / WithdrawnNot ApplicableIIT

RELISTOR's Effects on Opioid-Induced Constipation in Postoperative 1-2 Level Anterior Lumbar Interbody Fusion Patients: A Case-Control Study

This will be a prospective case-control study of 40 patients undergoing 1-2 level ALIF procedures at Methodist Dallas Medical Center (MDMC). Patient records will be reviewed to identify details including demographics, comorbidities, procedure details, and the primary and secondary outcome metrics.

Start Date01 Jul 2021

Sponsor / Collaborator

Methodist Health System, Inc.

100 Clinical Results associated with Dioctyl Sodium Sulfosuccinate

100 Translational Medicine associated with Dioctyl Sodium Sulfosuccinate

100 Patents (Medical) associated with Dioctyl Sodium Sulfosuccinate

5,542

Literatures (Medical) associated with Dioctyl Sodium Sulfosuccinate

01 Feb 2025·Life Science Alliance

Computing hematopoiesis plasticity in response to genetic mutations and environmental stimulations

Article

Author: Ma, Yunxi ; Li, Yanmei ; Cai, Lorie Chen ; He, Hang ; Wen, Yuchen ; Cai, Zhigang ; Zhao, Baobing ; Wang, Huaquan ; Bao, Dengyi

Cell plasticity (CP), describing a dynamic cell state, plays a crucial role in maintaining homeostasis during organ morphogenesis, regeneration, and trauma-to-repair biological process. Single-cell-omics datasets provide an unprecedented resource to empower CP analysis. Hematopoiesis offers fertile opportunities to develop quantitative methods for understanding CP. In this study, we generated high-quality lineage-negative single-cell RNA-sequencing datasets under various conditions and introduced a working pipeline named scPlasticity to interrogate naïve and disturbed plasticity of hematopoietic stem and progenitor cells with mutational or environmental challenges. Using embedding methods UMAP or FA, a continuum of hematopoietic development is visually observed in wild type where the pipeline confirms a lowproportion of hybrid cells(Phc, with bias range: 0.4∼0.6) on a transition trajectory. UponTet2mutation, a driver of leukemia, or treatment of DSS, an inducer of colitis,Phcis increased and plasticity of hematopoietic stem and progenitor cells was enhanced. We prioritized several transcription factors and signaling pathways, which are responsible forPhcalterations. In silico perturbation suggests knocking out EGR regulons or pathways of IL-1R1 and β-adrenoreceptor partially reversesPhcpromoted byTet2mutation and inflammation.

01 Jan 2025·Journal of Pharmaceutical and Biomedical Analysis

Altered gut metabolites and metabolic reprogramming involved in the pathogenesis of colitis-associated colorectal cancer and the transition of colon "inflammation to cancer"

Article

Author: Wang, Dunfang ; Chang, Hao ; Zhu, Lin ; Liu, Li ; Liu, Bin ; Feng, Xue ; Liu, Haifan ; Zhang, Caijuan ; Yang, Weipeng ; Yang, Lei ; Sun, Jingwei ; Li, Tao

Colitis-associated colorectal cancer (CAC) is fatal and can develop spontaneously or as a complication of inflammatory bowel diseases. Although co-administration of azoxymethane/dextran sulfate sodium (AOM/DSS) is a classic method for CAC modeling, its limitations need to be addressed. Accordingly, we aimed to optimize the AOM/DSS model to study CAC extensively and further investigate its pathogenic mechanisms relative to microbiota and metabolism. We optimized the CAC model via a single or enhanced injection of AOM combined with different administration modes and varying DSS concentrations. Subsequently, the fecal-microbiota composition was examined using 16S RNA sequencing, and fecal-colon-metabolome profiles were evaluated via ultra-high performance liquid chromatography-mass spectrometry. Two interval injections of AOM combined with 1.5 % DSS-free drinking resulted in a high tumor formation rate, uniform tumor formation, and low mortality. Based on this model, we innovatively divided the pathogenesis of CAC into three stages, namely inflammation induction, proliferation initiation, and tumorigenesis, and examined the pathological characteristics in each stage. Gut microbial dysbiosis and metabolic alteration drove colorectal tumorigenesis by aggravating inflammation while promoting cell proliferation and carcinogenesis in mice. For the first time, we dynamically demonstrated the process of colon "inflammation to cancer" transformation and provided novel insights to clarify the role of amino acid metabolism in the formation of CAC.

01 Jan 2025·Journal of Ethnopharmacology

Codonopsis pilosula polysaccharide alleviates ulcerative colitis by modulating gut microbiota and SCFA/GPR/NLRP3 pathway

Article

Author: Wei, Wenfeng ; Huo, Jinhai ; Wang, Weiming ; Yang, Qixin ; Zhou, Jiaxin

ETHNOPHARMACOLOGICAL RELEVANCECodonopsis pilosula (Franch.) Nannf. (CP) is a Chinese herb commonly used in traditional Chinese medicine to treat ulcerative colitis (UC). C. pilosula polysaccharide (CPPS) is an important bioactive compound in CP. Polysaccharides are degraded by and interact with the gut microbiota, exerting therapeutic effects. However, the mechanism of action of CPPS in treating UC by regulating gut microbiota is unclear.AIM OF THE STUDYThis study aimed to elucidate the therapeutic efficacy of CPPS on UC mice and its mechanism of action.MATERIALS AND METHODSSize-exclusion chromatography with multi-angle laser-light scattering and refractive index analysis was employed to ascertain the molecular weight of CPPS, while its monosaccharide composition was determined using ion chromatography. An experimental colitis mouse model was induced by administering 3% (dextran sulfate sodium) DSS in drinking water for five consecutive days. Three doses of CPPS were administered to evaluate their therapeutic effects on UC. CPPS was administered for seven days, and salicylazosulfapyridine was used as a positive control. Inflammatory cytokine secretion in the colon tissue was measured, and histopathological evaluation was performed on colon sections. Alterations in the abundance of the intestinal microbiota species were also analyzed. We then quantified short-chain fatty acids (SCFAs) in the cecal content and verified the G protein-coupled receptor (GPR)/nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) pathways using Western blot. Furthermore, the ameliorative effect of gut microbiota on DSS-induced UC symptoms was verified using the fecal microbiota transplantation (FMT) experiment.RESULTSCPPS comprised of rhamnose, arabinose, galactose, glucose, and galacturonic acid. CPPS significantly alleviated DSS-induced UC. Compared to the DSS group, CPPS treatment significantly increased the ratio of the Firmicutes to the Bacteroidetes and upregulated the abundance of beneficial bacteria such as g__Ligilactobacillus, g_Akkermansia, g_Faecalibaculum, g_Odoribacter. The release of acetic acid and butyric acid were further promoted. CPPS can inhibit NLRP3 activation by binding SCFAs to GPR proteins, thereby reducing intestinal inflammation. FMT confirmed that the gut microbiota in the CPPS-trans group sufficiently mitigated DSS-induced UC symptoms.CONCLUSIONSCPPS ameliorates the symptoms of DSS-induced UC primarily through the gut microbiota modulation and SCFA/GPR/NLRP3 pathways, making it a promising candidate for UC treatment.

News (Medical) associated with Dioctyl Sodium Sulfosuccinate

21 May 2024

·www.biospace.com

Palisade Bio’s Lead Product Candidate, PALI-2108 Demonstrates Local Bioactivation and Dose Dependent Efficacy Response in Preclinical Mouse Models

Data presented at Digestive Disease Week (DDW) 2024 Preclinical data demonstrate PALI-2108 to be safe, effective, and well tolerated PALI-2108 is orally delivered and colon-specific allowing for local activity with low systemic exposure PALI-2108 exhibited a dose-dependent efficacy response in two DSS colitis mouse models, achieving efficacy comparable to doses of apremilast considered intolerable for human use in Ulcerative Colitis (UC) patients Company on track to commence Phase 1 human clinical study of lead product candidate, PALI-2108, for the treatment of UC before year end Carlsbad, CA, May 21, 2024 (GLOBE NEWSWIRE) -- Palisade Bio, Inc. (Nasdaq: PALI) (“Palisade” or the “Company”), biopharmaceutical company focused on developing and advancing novel therapeutics for patients living with autoimmune, inflammatory, and fibrotic diseases, today announced the presentation of positive preclinical data from PALI-2108, an orally administered, locally acting colon-specific Phosphodiesterase-4 (PDE4) inhibitor prodrug in development for patients affected by UC, at DDW 2024 being held in Washington, D.C., May 18-21, 2024. The poster titled, “Local Bioactivation and efficacy of PALI-2108: A Promising PDE4 Inhibitor Prodrug for Ulcerative Colitis Treatment,” is being presented by Dr. Mitch Jones as part of the Animal Models of IBD: Pre-Clinical Treatment of Intestinal Inflammation session being held today, May 21, 2024. The poster is available on the Scientific Publications page of the Company’s website. “The findings from this preclinical study add to our growing body of encouraging data for PALI-2108 and further bolster our confidence in its potential in the treatment of UC,” commented Dr. Mitch Jones, CMO of Palisade Bio. “Based on the data demonstrated to date, we believe PALI-2108 has the potential to be the first approved PDE4 inhibitor for UC and importantly, provide a much-needed solution for patients.” The preclinical data highlighted in the poster reveal significant advancements in assessing on-target PDE4 binding within colon tissue homogenates when dosed with apremilast, PALI-2108, or Vehicle, utilizing a classic cellular thermal shift assay (CETSA) to detect changes in thermal stability. To comprehensively evaluate PALI-2108's efficacy across various doses, researchers employed an acute colitis model in mice induced by 4% DSS in drinking water from Day 1 to Day 8. Mice received twice-daily (BID) treatments of PALI-2108 at 20, 40, and 80 mg/kg/dose BID, while cyclosporin A and apremilast were administered at 40 and 12.5 mg/kg/dose BID, respectively. The assessment of DSS-induced colitis included monitoring Body Weight score, Stool Consistency score, and Fecal Blood score from Day 1 to Day 8, with evaluations conducted 1 to 2 hours post-dosing. Overall disease state was measured using a Disease Activity Index (DAI) score, calculated by pooling the three in-life scores, assessed daily from Days 1 to 8. Furthermore, a single oral dose of the prodrug PALI-2108 at 43 mg/kg and active PALI-0008 at 0.1, 0.3, 1, and 3 mg/kg was administered to dogs, with a focus on monitoring key clinical adverse events, including emesis. Remarkably, the PALI-2108 prodrug prevented emesis observed with lower doses of the PDE4 active moiety in the model, demonstrating an enhanced therapeutic window. Key Findings PALI-2108 demonstrates similar target engagement to the PDE4 inhibitor, apremilast, which is approved for use in psoriasis and psoriatic arthritis. In a DSS colitis mouse model, PALI-2108 significantly prevented colon length reduction in dose dependent manner, and showed dose dependent improvements in body weight score, stool consistency score, fecal blood score, overall disease activity index (DAI) score, and AUC of DAI over the course of the study. Importantly, PALI-2108 exhibited a dose-dependent efficacy response in two DSS colitis mouse models, achieving efficacy comparable to doses of apremilast considered intolerable for human use in UC patients. No systemic toxicity in dogs and large therapeutic window due to local activation. About Palisade Bio Palisade Bio is a biopharmaceutical company focused on developing and advancing novel therapeutics for patients living with autoimmune, inflammatory, and fibrotic diseases. The Company believes that by using a targeted approach with its novel therapeutics it will transform the treatment landscape. For more information, please go to . Forward Looking Statements This communication contains “forward-looking” statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding the Company’s intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things: the extent of our cash runway; our ability to successfully develop our licensed technologies; estimates about the size and growth potential of the markets for our product candidates, and our ability to serve those markets, including any potential revenue generated; future regulatory, judicial, and legislative changes or developments in the United States (U.S.) and foreign countries and the impact of these changes; our ability to maintain the Nasdaq listing of our securities; our ability to build a commercial infrastructure in the U.S. and other markets; our ability to compete effectively in a competitive industry; our ability to identify and qualify manufacturers to provide API and manufacture drug product; our ability to enter into commercial supply agreements; the success of competing technologies that are or may become available; our ability to attract and retain key scientific or management personnel; the accuracy of our estimates regarding expenses, future revenues, capital requirements and needs for additional financing; our ability to obtain funding for our operations; our ability to attract collaborators and strategic partnerships; and the impact of the COVID-19 pandemic or any global event on our business, and operations, and supply. Any statements contained in this communication that are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements are based upon the Company’s current expectations. Forward-looking statements involve risks and uncertainties. The Company’s actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, the Company’s ability to advance its nonclinical and clinical programs, the uncertain and time-consuming regulatory approval process; and the Company’s ability to secure additional financing to fund future operations and development of its product candidates. Additional risks and uncertainties can be found in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2023, filed with the Securities and Exchange Commission (“SEC”) on March 26, 2024. These forward-looking statements speak only as of the date hereof and the Company expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in the Company’s expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based. Investor Relations Contact JTC Team, LLC Jenene Thomas 833-475-8247 PALI@jtcir.com Source: Palisade Bio

Clinical ResultPhase 1

22 May 2023

·www.sciencedaily.com

Study may explain why high-sugar diets can worsen IBD

Excess sugar hampers cells that renew the colon's lining in a mouse model of inflammatory bowel disease (IBD), according to a new study that could help get to the bottom of why limiting sugary foods can ease symptoms for patients with IBD. Excess sugar hampers cells that renew the colon's lining in a mouse model of inflammatory bowel disease (IBD), according to a new study by University of Pittsburgh scientists. The findings, published in Cellular and Molecular Gastroenterology and Hepatology, could help get to the bottom of why limiting sugary foods can ease symptoms for patients with IBD. "The prevalence of IBD is rising around the world, and it's rising the fastest in cultures with industrialized, urban lifestyles, which typically have diets high in sugar," said senior author Timothy Hand, Ph.D., associate professor of pediatrics and immunology at Pitt's School of Medicine and UPMC Children's Hospital of Pittsburgh. "Too much sugar isn't good for a variety of reasons, and our study adds to that evidence by showing how sugar may be harmful to the gut. For patients with IBD, high-density sugar -- found in things like soda and candy -- might be something to stay away from." Led by Ansen Burr, Ph.D., a student in Pitt's Medical Scientist Training Program, the researchers started by feeding mice either a standard or high-sugar diet. Then they mimicked symptoms of IBD by treating the animals with a chemical called DSS that causes damage to the colon. To their shock, all the mice on the high-sugar diet died within nine days. In contrast, all the animals on the standard diet survived until the end of the 14-day experiment. To learn what made sugar so deadly in mice with IBD symptoms, the team looked at the animals' colons. Also known as the large intestine, the colon is lined with a layer of epithelial cells that are arranged in finger-like projections called crypts. In a healthy colon, these cells are continually replenished by dividing stem cells at the bottom of each crypt. "The colon epithelium is like a conveyor belt," said Hand, who is also director of Pitt's Gnotobiotic Animal Core Laboratory. "It takes five days for cells to travel through the circuit from the bottom to the top of the crypt, where they are shed into the colon and defecated out. You essentially make a whole new colon every five days." When mice on the high-sugar diet were given DSS, that circuit collapsed, said Hand. In some of the animals, the protective layer of epithelial cells was completely lost, causing the colon to be full of blood and immune cells. Unexpectedly, a high-sugar diet was similarly lethal in germ-free mice treated with DSS, showing that sugar affects the colon directly and is not dependent on the gut microbiome as the researchers had predicted. Next, the team tested how sugar affected mouse and human colonoids, poppy seed-sized miniature intestines that can be grown in a lab dish. As concentrations of glucose, sucrose or fructose increased, fewer colonoids developed and they grew slower, evidence that sugar impaired cell division. "We found that stem cells were dividing much more slowly in the presence of sugar -- likely too slow to repair damage to the colon," said Hand. "The other strange thing we noticed was that the metabolism of the cells was different. These cells usually prefer to use fatty acids, but after being grown in high-sugar conditions, they seemed to get locked into using sugar." In sugary conditions, the cells had vastly altered metabolic pathways, and they produced lower levels of ATP, the energy-providing molecule that drives cellular processes. The researchers suspect that this rewiring of cellular pathways inhibits the capacity of stem cells to divide, slowing renewal of the colon lining and accelerating gut damage in IBD. According to Hand, these findings could help explain other research that has linked sweetened beverages, including sodas, soft drinks and juices, to negative outcomes in IBD patients. "If you eat an apple or an orange, you're eating a lot of sugar, but that sugar is tied up in the fruit's cells, so it takes a long time to digest and open up those cells to get the sugar," said Hand. "Whereas if you drink a soda, the sugar is available almost the second it hits your intestine, and it's easy to drink a huge amount of sugar in a very short time. Our research suggests that consuming high levels of sugar could have negative outcomes for repairing the colon in patients with inflammatory bowel disease." Hand said that future research, done in in collaboration with coauthor Semir Beyaz, Ph.D., assistant professor at Cold Spring Harbor Laboratory, will focus on understanding how diet and immune response can affect IBD. "I think that we need to investigate more deeply what diets are going to benefit patients who have intestinal damage, whether that be from IBD or from radiation therapy to treat colon cancer," said Hand. "It's about a nutraceutical approach to colon damage, or the idea of finding the right diet for a particular patient." Other authors on the study were Junyi Ji, B.Med., of Tsinghua University; Kadir Ozler, B.S., Onur Eskiocak, B.S., and Brian Yueh, B.S., of Cold Spring Harbor Laboratory; and Heather L. Mentrup, Ph.D., Rachel Cumberland, B.A., Ashley V. Menk, B.S., Natalie Rittenhouse, B.S., Chris W. Marshall, Ph.D., Pailin Chiaranunt, B.S., Xiaoyi Zhang, M.D., Ph.D., Lauren Mullinax, M.D., Abigail Overacre-Delgoffe, Ph.D., Vaughn S. Cooper, Ph.D., Amanda C. Poholek, Ph.D., Greg M. Delgoffe, Ph.D., and Kevin P. Mollen, M.D., all of Pitt or UPMC. This work was supported by the Richard King Mellon Institute for Pediatric Research, the National Institutes of Health (T32AI089443-10), the Damon Runyon Cancer Research Foundation (2360-19), the Kenneth Rainin Foundation and the Cancer Center Support Grant (5P30CA045508).

29 Oct 2019

·www.globenewswire.com

The global dioctyl maleate market was valued at $242.6 million in 2018, and is projected to reach $326.1 million by 2026, growing at a CAGR of 3.7% from 2019 to 2026

New York, Oct. 29, 2019 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Dioctyl Maleate Market by End Use : Global Opportunity Analysis and Industry Forecast, 2019-2026" - The global dioctyl maleate market was valued at $242.6 million in 2018, and is projected to reach $326.1 million by 2026, growing at a CAGR of 3.7% from 2019 to 2026. Dioctyl maleate (DOM) is a maleic acid, which acts as a non-phthalate plasticizer, and is used in resins to provide flexibility and elasticity. These types of polymerizations with dioctyl maleate occur during the production of adhesives, emulsion paints, surfactants, textile coatings, and wetting agents. In particular, DOM is used as a chemical intermediate in the production of surfactant sodium dioctyl sulfosuccinate, which is a used as a wetting agent for detergent. The growth of the global dioctyl maleate market is majorly driven by increase in demand for surfactants, which find their application across industries such as soaps & detergents, personal care, lubricants and fuel additives, industry & institutional cleaning, food processing, and oilfield chemicals. In addition, DOM is applicable in the manufacture of sulfosuccinates, which are used as wetting agents for detergent applications. DOM acts as a non-phthalate plasticizer, and is used in automobiles to join the various parts, thereby replacing the use of metal nuts & bolts and reducing the overall weight of the vehicle. Increase in the demand for lightweight and higher fuel-efficient vehicles is expected to boost the demand for non-phthalate plasticizers, which in turn will drive the growth of the global dioctyl maleate market. Moreover, upsurge in demand for packaged food by consumers owing to hectic schedule and changes in eating habits is expected to augment the need for food contact cling films. This is attributed to significantly contribute toward the growth of global market, as dioctyl maleate is used in the manufacturing of food contact cling films. The demand for food contact cling films is further anticipated to grow at a considerable rate, as they enhance the shelf life of food products. However, availability of large number of substitutes such as dioctyl phthalate (DOP), dioctyl adipate (DOA), and dibutyl maleate (DBM) at lower prices is expected to hinder the growth of this market. On the contrary, implementation of stringent government regulations on usage of phthalates is expected to offer lucrative opportunity for market expansion, as dioctyl maleate acts as non-phthalate plasticizer, which is nontoxic in nature. The global dioctyl maleate market is segmented based on end use and region. Depending on end use, the market is classified into adhesives, emulsion paint, surfactants & wetting agent, plasticizer, textile coating, and others. Region wise, it is analyzed across North America (U.S., Canada, and Mexico), Europe (Germany, France, Italy, Spain, UK, and rest of Europe), Asia-Pacific (China, India, Japan, South Korea, India, and rest of Asia-Pacific), and LAMEA (Brazil, Saudi Arabia, South Africa, and rest of LAMEA). The key players operating in the dioctyl maleate industry include Biesterfield AG, Celanese Corporation, ESIM Chemicals, HallStar, Hangzhou Qianyang Technology Co., Ltd, Henan GP Chemicals Co., Ltd., Merck KGaA, Polynt SpA, Shandong Yuanli Science and Technology Co., Ltd., and Tokyo Chemical Industry Co., Ltd. KEY BENEFITS FOR STAKEHOLDERS • Porter’s five forces analysis helps analyze the potential of buyers & suppliers and the competitive scenario of the industry for strategy building. • It outlines the current trends and future scenario of the market from 2019 to 2026 to understand the prevailing opportunities and potential investment pockets. • Major countries in the region have been mapped according to their individual revenue contribution to the regional market. • The key drivers, restraints, and opportunities and their detailed impact analysis are elucidated in the study. • The profiles of key players along with their key strategic developments are enlisted in the report. KEY MARKET SEGMENTS • By End Use • Adhesives, • Emulsion paint • Surfactants & wetting agent • Plasticizer • Textile coating • Others • By Region • North America o U.S. o Canada o Mexico • Europe o Germany o France o Italy o Spain o UK o Rest of Europe • Asia-Pacific o China o Japan o India o South Korea o Rest of Asia-Pacific • LAMEA o Brazil o Saudi Arabia o South Africa o Rest of LAMEA Read the full report: About Reportlinker ReportLinker is an award-winning market research solution. Reportlinker finds and organizes the latest industry data so you get all the market research you need - instantly, in one place. __________________________ Clare: clare@reportlinker.com US: (339)-368-6001 Intl: +1 339-368-6001

100 Deals associated with Dioctyl Sodium Sulfosuccinate

External Link

KEGG	Wiki	ATC	Drug Bank
-	Dioctyl Sodium Sulfosuccinate	A06AA02	DB11089

R&D Status

Approved

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Indication	Country/Location	Organization	Date
Constipation	-	-	-
Hemorrhoids	-	-	-
Pharmaceutical aids	-	-	-

Developing

10 top R&D records.

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Indication	Highest Phase	Country/Location	Organization	Date
Acne Vulgaris	Preclinical	US	Meditech Pharmaceuticals, Inc.	-
Herpes Simplex	Preclinical	US	Meditech Pharmaceuticals, Inc.	-

Clinical Result

Indication

Phase

Evaluation

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Study	Phase	Population	Analyzed Enrollment	Group	Results	Evaluation	Publication Date


DDW2023	Not Applicable	-	-	Dextran sulfate sodium (Control rats)	wscdzyheva(miuefuchwo) = reduced by 33% in DSS-treated male and female rats tktcfoaykk (ytnzzakdfl ) View more	-	06 May 2023
				DSSDextran sulfate sodium (DSS-treated rats)
NCT03523715 (CTgov)	Phase 4	Constipation	77	Prunes+Docusate Sodium (Prunes)	cmrdgdkuqx(tzelsacdwo) = csaewnctwr feaguyjfgv (ttaxjtxepq, csncpzozgu - unujvarokt) View more	-	08 Apr 2021
				Docusate Sodium (Control)	cmrdgdkuqx(tzelsacdwo) = mbrdetzllm feaguyjfgv (ttaxjtxepq, deebndlgso - pdjijkaolt) View more
NCT01044212 (CTgov)	Not Applicable	Intestinal Diseases	72	Polyethylene glycol+Dulcolax+Colace	ehhetmfevf(mrtamfdmdg) = vhpitmgbdn rjamalnstd (ksipmiulkk, sdguduwcit - rzxpnhzpvq) View more	-	21 Oct 2015
UEGW	Not Applicable	-	-	Saline	keomboyzem(cvtmtkyjqv) = mvdlywtosb lwpzclijmz (vzbfgsfkuc )	-	01 Oct 2014
				DSS in drinking water	keomboyzem(cvtmtkyjqv) = gvrnopzsjl lwpzclijmz (vzbfgsfkuc )

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