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Clinical Trial Summary

Evaluate the diagnostic performance of the Gyni™ device to detect different vaginitis conditions by comparison to microscopic diagnosis and related lab tests.


Clinical Trial Description

During gynecological exams, vaginal discharge samples will be are taken for testing the pH level, microscopic examination and laboratory examinations (vaginal cultures and sexually transmitted infections). One additional sample will be taken intended for the Gyni™ system diagnosis. This additional examination will be performed in the clinic by pulling the cytobrush through a dedicated cartridge and scanning it in the Gyni table-top scanner. The result diagnosis will be anonymously kept in the cloud. The diagnosis suggested by the Gyni system will not be visible to the physician in order to prevent any bias. Results from the physician, from the device and from the lab will be summarized and compared by the chief investigator ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04219605
Study type Observational
Source Meir Medical Center
Contact Ahinoam Lev-Sagie, MD
Phone 972-2-5889551
Email levsagie@netvision.net.il
Status Recruiting
Phase
Start date December 1, 2020
Completion date December 2023

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