RecruitingNot ApplicableNCT06480604

Effect of a Multi-strain Probiotic on Recurrent Vulvovaginal Candidiasis

A Pilot Clinical Trial Assessing the Effect of a Multi-strain Probiotic on the Risk of Recurrence and Severity of Symptoms in Females With Recurrent Vulvovaginal Candidiasis


Sponsor

The Archer-Daniels-Midland Company

Enrollment

126 participants

Start Date

Oct 15, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study evaluates the effect of a multi-strain probiotic on the risk of recurrence and severity of symptoms in females with recurrent vulvovaginal candidiasis (R-VVC).


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Placebo and Probiotic for people with vulvovaginal candidiasis. The study is currently recruiting participants at 6 locations. People eligible for this study include women aged 18 Years to 50 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTProbiotic

Participants in this arm will receive a daily dose of 2x10\^9 Colony Forming Units (CFU) of a multi strain probiotic (live bacterium), corresponding to 2 capsules once daily, for 6 months.

DIETARY_SUPPLEMENTPlacebo

Participants in this arm will receive an equivalent placebo for the duration of the study (6 months).


Locations(6)

Anand Multispeciality Hospital

Vadodara, Gujarat, India

Life Care Hospital

Nashik, Maharashtra, India

AMF's Moraya Multispeciality Hospital

Pune, Maharashtra, India

ENT & Vertigo Clinic

Pune, Maharashtra, India

Vivaan Hospital

Sopāra, Maharashtra, India

Matritva Women's Hospital

Vasai, Maharashtra, India

View Full Details on ClinicalTrials.gov

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NCT06480604


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