Clinical Trials Directory

Trials / Completed

CompletedNCT06392529

Efficacy of Voriconazole Loaded Spanlastics Gel Versus Clotriamazole Cream on Treating Vulvovaginal Candidasis

Status
Completed
Phase
Study type
Observational
Enrollment
28 (actual)
Sponsor
Beni-Suef University · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers

Summary

To investigate and compare the efficacy of voriconazole loaded spanlastics (VCZ loaded SPs) optimum gel formula (F2 VCZ loaded SP gel) versus Clotrimazole cream in treating candida albicans causing vulvovaginal candidiasis for different durations of 3 days and 5 days.

Detailed description

The current study will be prospective controlled randomized clinical trial. 28 female patients suffering from vulvovaginal candidiasis will be enrolled in the following 2 groups: Gp 1 (Test group): including 14 patients with vulvovaginal candidiasis albicans that will be randomized in the following subgroups: Gp 1a: will be treated with F2 VCZ loaded SP gel for 3 days. Gp 1 b: Will be treated with F2 VCZ loaded SP gel for 5 days. Gp 2 (Control group): including 14 patients with vulvovaginal candidiasis albicans will be randomized in the following sub groups Gp 2 a: will be treated with the Clotrimazole cream available in the market for 3 days. Gp 2 b: Will be treated with the Clotrimazole cream available in the market for 5 days. Smears will be taken from the patients before starting the therapeutic protocol and after finishing it. Compliance of the patients to the creams will be assesses

Conditions

Interventions

TypeNameDescription
DRUGVoriconazole PowderThe drug will be topically applied for vagina of patients suffering from vaginal Candidasis albican

Timeline

Start date
2024-05-10
Primary completion
2024-06-15
Completion
2024-06-30
First posted
2024-04-30
Last updated
2024-08-07

Locations

1 site across 1 country: Egypt

Regulatory

Source: ClinicalTrials.gov record NCT06392529. Inclusion in this directory is not an endorsement.