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Completed Phase 3 Interventional Results available

A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate Vaginal Cream 2% (Watson Laboratories, Inc.) to Clindesse® (Ther-Rx™, Clindamyin Phosphate Vaginal Cream 2%) and Both Active Treatments to a Placebo Control in the Treatment of Bacterial Vaginosis in Non-pregnant Women

ClinicalTrials.gov ID: NCT02210689

Public ClinicalTrials.gov record NCT02210689. 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 22, 2026, 3:12 AM EDT

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

Study identification

NCT ID
NCT02210689
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Actavis Inc.
Industry
Enrollment
604 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
Dec 31, 2013
Primary completion
Sep 30, 2014
Completion
Nov 30, 2014
Last update posted
Jan 27, 2020

2014

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Akesis Investigator site 5 Birmingham Alabama
Akesis Investigator site 12 La Mesa California
Akesis investigator site 6 San Diego California
Akesis Investigator site 1 Boynton Beach Florida
Akesis investigator site 14 North Miami Florida
Akesis investigator site 17 Sanford Florida 32771
Akesis investigator site 8 Sunrise Florida
Akesis Investigator site 10 West Palm Beach Florida
Akesis Investigator site 9 Roswell Georgia
Akesis Investigator site 15 Metairie Louisiana
Akesis investigator site 16 Lawrenceville New Jersey
Akesis investigator site 11 Port Jefferson New York
Akesis investigator site 13 Philadelphia Pennsylvania
Akesis Investigator site 7 Jackson Tennessee
Akesis investigator site 18 Houston Texas 77011

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02210689, 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 Jan 27, 2020 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02210689 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →