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Clinical Trial Summary

Women diagnosed with Vulvovaginal Candidiasis by the health care professional will be enrolled in the study. All participants should fulfil inclusion and exclusion criteria. The study product will be used for 5 days, once a day. The doctor will evaluate the patients before and at the end of the treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05552378
Study type Interventional
Source Karo Pharma AB
Contact
Status Completed
Phase N/A
Start date February 20, 2023
Completion date April 5, 2023

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