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Completed Phase 3 Interventional

A Therapeutic Equivalence Study of Two Metronidazole Gel 1% Topical Treatments of Rosacea

ClinicalTrials.gov ID: NCT02393937

Public ClinicalTrials.gov record NCT02393937. 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, 6:58 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 Multi-center, Double-blind, Randomized, Vehicle-controlled, Parallel-group Study Comparing Metronidazole Gel 1%, to Metrogel® (Metronidazole Gel) 1% in the Treatment of Rosacea

Study identification

NCT ID
NCT02393937
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
bioRASI, LLC
Industry
Enrollment
963 participants

Conditions and interventions

Interventions

  • Reference: Metronidazole Gel 1% Drug
  • Test: Metronidazole Gel 1% Drug
  • Placebo Gel Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jan 31, 2015
Primary completion
Jun 30, 2015
Completion
Sep 30, 2015
Last update posted
Sep 2, 2020

2015

United States locations

U.S. sites
27
U.S. states
13
U.S. cities
26
Facility City State ZIP Site status
Not listed Los Angeles California 90036
Not listed San Diego California 92121
Not listed Boca Raton Florida 33486
Not listed Clearwater Florida 33761
Not listed Miami Florida 33126
Not listed Miami Florida 33136
Not listed Miramar Florida 33027q
Not listed Ocala Florida 34471
Not listed Tampa Florida 33634
Not listed Lexington Kentucky 40509
Not listed Watertown Massachusetts 02472
Not listed Las Vegas Nevada 89104
Not listed New York New York 10075
Not listed High Point North Carolina 27262
Not listed Raleigh North Carolina 27612
Not listed Cincinnati Ohio 45246
Not listed Philadelphia Pennsylvania 19103
Not listed Warwick Rhode Island 02886
Not listed Mt. Pleasant South Carolina 29464
Not listed Austin Texas 78759
Not listed El Paso Texas 79902
Not listed Houston Texas 77055
Not listed Pflugerville Texas 78660
Not listed Plano Texas 75093
Not listed San Antonio Texas 78229
Not listed Arlington Virginia 22203
Not listed Norfolk Virginia 23507

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 NCT02393937, 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 Sep 2, 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 NCT02393937 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →