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Clinical Trial Summary

Open, single arm trial that intends to confirm the safety and efficacy of Multi-Gyn ActiGel Plus for treatment of Bacterial Vaginosis. Adult women will be diagnosed by the gynaecologist based on the Amsel criteria at day 0. They will use the product for 7 days and will come to the practice at day 21. The primary endpoint is the clinical cure rate of Bacterial Vaginosis at 3 weeks after start of treatment.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05211921
Study type Interventional
Source Karo Pharma AB
Status Completed
Phase N/A
Start date December 7, 2021
Completion date May 11, 2022

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