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Effect of Ultra-gyn® on Vulvovaginal Candidiasis - Trial NCT05273333

Access comprehensive clinical trial information for NCT05273333 through Pure Global AI's free database. This phase not specified trial is sponsored by Biocodex and is currently Recruiting. The study focuses on Vulvovaginal Candidiasis, Genital. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.govNCT05273333
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Effect of Ultra-gyn® on Vulvovaginal Candidiasis

Study Focus

Ultra-gyn®

Interventional

device

Sponsor & Location

Biocodex

Quatre Bornes, Mauritius

Timeline & Enrollment

N/A

Feb 23, 2022

Dec 01, 2022

30 participants

Primary Outcome

To assess the effect of Ultra-gyn® in relieving the symptoms of Vulvovaginal Candidiasis

Summary

The aim of this post-market clinical follow up study is to confirm the performance and the
 safety of Ultra-gyn® (when used in accordance with its approved labelling)

ICD-10 Classifications

Candidiasis of vulva and vagina
Candidiasis, unspecified
Candidiasis
Candidiasis of other urogenital sites
Abscess of vulva

Data Source

ClinicalTrials.gov

NCT05273333

Device Trial