Rosacea Clinical Trial - Clinical Trial to Evaluate the Effect of a

Status Recruiting

Clinical Trial Summary

The clinical trial has a randomized, double-blind, placebo-controlled design, in which the aim is to evaluate the effect of a probiotic mix, with a 12-week treatment, on the evolution of rosacea. This 12 weeks of treatment are structured into three visits: Visit 1 (initial; week 0), Visit 2 (intermediate; week 6) and Visit 3 (final; week 12).

Clinical Trial Description

The three visits that make up the study and the actions to be carried out in each of them are described below: Visit 1 (initial; week 0) Once the informed consent is signed, a doctor trained for the study performs the initial interview where it is verified that the patient meets all the inclusion criteria and none of the exclusion criteria and their medical history.The investigator will proceed to assign the patient the next study participant number and, according to a previously prepared randomization list, the treatment that they will receive during the study will be assigned. The investigator will assess the severity and symptoms of rosacea according to the Investigator's Global Assessment (IGA) and Clinician Erythema Assessment (CEA) scales. The patient will also complete a questionnaire to assess the impact on quality of life due to the disease: Dermatology Life Quality Index (DLQI). Visit 2 (intermediate; week 6) In this intermediate visit, in addition to assessing the symptoms of the disease with the detailed scales, the investigator will record the adverse events reported by the patient, as well as the concomitant treatments used. Also, the treatment compliance rate will be calculated by counting the capsules returned by the patient. Visit 3 (final; week 12) In the final visit, the same actions will be carried out as in the intermediate visit, evaluating the severity of the disease and the remaining capsules will be collected, to calculate treatment compliance, concomitant treatments and adverse events. Visit 4 (post-treatment follow-up; week 24) During this visit, the symptoms of the disease will be assessed with the two scales used in the study and the treatments that the patient has required during the 12 weeks after the end of the study treatment will be counted. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05815511
Study type	Interventional
Source	Bionou Research, S.L.
Contact	Laura Navarro Moratalla
Phone	+34 865780170
Email	laura.navarro@bioithas.com
Status	Recruiting
Phase	N/A
Start date	April 4, 2022
Completion date	July 4, 2024

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Clinical Trial to Evaluate the Effect of a Probiotic Mixture on the Rosacea Evolution

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms