/ CompletedNot Applicable Clinical Trial for the Evaluation of I+Med's DayDrop Advanced Ophthalmic Drop in Improving Signs and Symptoms of Mild/Moderate Dry Eye
Clinical trial conducted with the aim of evaluating changes in the signs of dry eye through the change in the amount of tears produced, measured through the Schirmer test. It will be performed in 45 patients diagnosed with mild/moderate dry eye who meet the inclusion/exclusion criteria. Follow-up will be 12 weeks with a maximum of 4 visits.
/ CompletedNot Applicable Post-marketing Study for the Evaluation of the Efficacy and Safety of Profilm Cold Sores
Experimental clinical study with a post-marketing, prospective, intra-subject controlled design to evaluate the efficacy and safety of the use of a medical device for the treatment of cold sores, over a maximum period of two weeks (or until the outbreak has resolved).
/ CompletedNot Applicable Post-marketing Study for the Evaluation of the Efficacy and Safety of Profilm Mouth Sores
The study aims to assess the effect of Profilm Mouth Sores treatment for relieving symptoms caused by mouth sores. It will involve 35 participants and last around 14 days or until the sores heal, with three daily applications. A dermatology specialist will evaluate the results through tests and examinations of the treated area.
100 Clinical Results associated with I+MED, S.COOP
0 Patents (Medical) associated with I+MED, S.COOP
100 Deals associated with I+MED, S.COOP
100 Translational Medicine associated with I+MED, S.COOP