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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 Oct 27, 2026, 6:51 AM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to compare the efficacy of two Metronidazole Gels 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

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
Feb 2015 (Type not available)
Primary completion
Jul 2015 (Actual)
Completion
Oct 2015 (Actual)
Last update posted
Sep 3, 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 3, 2020 · Synced Oct 27, 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 public registry record, listed eligibility criteria, and available contact information for NCT02393937 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →