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Completed No phase listed Observational

Non-Interventional Extension to Investigate Recurrence of Vulvovaginal Candidiasis and Candida Colonization

ClinicalTrials.gov ID: NCT02888197

Public ClinicalTrials.gov record NCT02888197. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:50 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Non-Interventional Extension Study to Investigate Vulvovaginal Candidiasis Recurrence and Candida Colonization Following a Phase 2 Randomized, Active-Controlled Study of Two Formulations of CD101 Compared to Fluconazole for the Treatment of Moderate to Severe Episodes of Acute Vulvovaginal Candidiasis

Study identification

NCT ID
NCT02888197
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Cidara Therapeutics Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Industry
Enrollment
32 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 15, 2016
Primary completion
Mar 14, 2017
Completion
Mar 14, 2017
Last update posted
Mar 1, 2018

2016 – 2017

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Precision Trials AZ Phoenix Arizona 85032
The Women's Clinical, P.A. Little Rock Arkansas 72205
Women's Health Care Research Corp San Diego California 92111
Olympian Clinical Research Clearwater Florida 33756
Women's Medical Research Clearwater Florida 33759
Altus Research Inc Lake Worth Florida 33461
New Age Medical Research Corporation Miami Florida 33186
Augusta University Augusta Georgia 30912
Clinical Trials Management LLC Metairie Louisiana 70006
Wayne State University Detroit Michigan 48201
Saginaw Valley Medical Research Group LLC Saginaw Michigan 48604
Lawrence OB GYN Clinical Research LLC Lawrenceville New Jersey 08648
Alliance Women's Research Group LLC Riverside Park New Jersey 08075
Soffolk OB/GYN Port Jefferson New York 11777
Eastern Carolina Women's Center New Bern North Carolina 28562
Hawthorne Medical Research Inc Winston-Salem North Carolina 27103
Unified Women's Clinical Research - Hickory Winston-Salem North Carolina 27103
Women's Health Research Columbus Ohio 43123
Drexel University Philadelphia Pennsylvania 19102
TMC Life Research Inc. Houston Texas 77054
Clinical Trials of Texas Inc San Antonio Texas 78229
Tidwewater Physicians for Women Norfolk Virginia 23502
Seattle Women's Health, Research, Gynecology Seattle Washington 98105

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02888197, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 1, 2018 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02888197 live on ClinicalTrials.gov.

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