Clinical Protocol CERN Feasibility Study

Recruiting N/A Interventional Study
Bacterial Vaginosis Fungal Vaginal Infections
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
9 (estimated)
Sponsor
Cern Corporation · Industry
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About This Trial
The goal of this clinical trial is to learn if the intravaginal Cern device works to treat bacterial vaginosis and fungal vaginitis in premenopausal women. It will also learn about the safety of the device. The main questions it aims to answer are: Does the device accomplish symptom resolution and negative diagnostic tests post-treatment? What medical problems do participants have when using the i…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Confirm symptomatic and laboratory-confirmed bacterial vaginosis or fungal vaginitis Exclusion Criteria: * Postmenopausal status, current use of intravaginal devices, concurrent medical therapy for fungal vaginitis or bacterial vaginosis, recent medical therapy for vaginitis…
Contacts

Gregg Klang

(949) 306-7160

gklang@cerndevice.com

CONTACT

Melanie Santos

(650) 353-6353

melaniesant@gmail.com

CONTACT