Actively Recruiting
The Effect of Medical Grade Honey Formulation (L-Mesitran) Administration on Recurrent Vulvovaginal Candidiasis Symptoms
Led by Maastricht University Medical Center · Updated on 2023-05-17
252
Participants Needed
2
Research Sites
243 weeks
Total Duration
On this page
Sponsors
M
Maastricht University Medical Center
Lead Sponsor
Z
Zuyderland Medical Centre
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of the study is to investigate the efficacy of Fluconazol versus L-Mesitran in the treatment of patients with recurrent vulvovaginal candidiasis. Vaginal swabs will be analyzed after 1, 6 and 12 months. The study ends after 252 included patients completed the study.
CONDITIONS
Official Title
The Effect of Medical Grade Honey Formulation (L-Mesitran) Administration on Recurrent Vulvovaginal Candidiasis Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women of at least 18 years old
- At least 3 episodes of vulvovaginal candidiasis symptoms in the last year
- Clinical and microbiological diagnosis of recurrent vulvovaginal candidiasis at consultation
- Ability to understand, consent, and follow trial procedures
You will not qualify if you...
- Mixed vaginal infections
- Pregnancy or planning pregnancy during the study
- Use of systemic or topical antifungal medication in the 2 weeks before inclusion
- Known allergy or contraindication to Fluconazole or honey
- Candida resistant to Fluconazole
- Breastfeeding women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Zuyderland Medical Centre
Heerlen, Netherlands
Actively Recruiting
2
MaastrichtUMC
Maastricht, Netherlands
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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