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Clinical Trial Summary

To assess the efficacy and safety of the use of probiotics as food supplements in reducing the SCORAD index in children with atopic skin compared with placebo. This is a randomized, placebo-controlled, double-blind clinical trial with 2 parallel groups, which will include 32 patients who attend some of the research centers. Patients will be randomized into one of the 2 study groups (allocation ratio 1: 1): Experimental group (Lactobacillus rhamnosus LRa05) and placebo group (placebo). The reduction of the SCORAD index, the number of sprouts in 12 weeks, the days of use of topical corticosteroids and one valuations of the skin condition (hydration).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05989295
Study type Interventional
Source Wecare Probiotics Co., Ltd.
Contact
Status Completed
Phase N/A
Start date January 26, 2022
Completion date April 21, 2023

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