Clin2
NCT06835361Possibly a fitRecruiting

Comparing two yeast infection treatments for women

Candidal Vulvovaginitis (ICD-10 Code: B37.3)Vulvovaginal Candidiasis (VVC)

Treatments studied

Part of Infections, Women’s health & pregnancy clinical trials.

This trial tests if a new combination vaginal suppository works better than the standard one for women with yeast infections. It aims to see if adding lactulose to clotrimazole helps clear the infection faster or more completely.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2/Phase 3
Enrollment
264 people
Ages
18 years to 60 years
Study type
Interventional

Who can take part

  • You are a woman between 18 and 60 years old.
  • You have a confirmed yeast infection (candidal vulvovaginitis).
  • You are not pregnant, not breastfeeding, and will use reliable birth control during the study and for 30 days after.
  • You have not used antibiotics or antifungal pills or creams in the last 2 weeks.
  • You do not have bacterial vaginosis or other chronic conditions of the female organs.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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