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Completed Phase 1 Interventional

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

ClinicalTrials.gov ID: NCT01513863

Public ClinicalTrials.gov record NCT01513863. 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 Sep 12, 2026, 2:20 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 Randomized, Double-Blind, Placebo Controlled, Parallel Design, Multi-Site Clinical Study to Compare the Bioequivalence of Two Metronidazole 1% Topical Gel Formulations in Patients With Moderate to Severe Rosacea

Brief summary

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

The objective of this study is to demonstrate that metronidazole 1% topical gel is effective for the treatment of patients with moderate to severe rosacea.

Study identification

NCT ID
NCT01513863
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
602 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
Jul 31, 2011
Primary completion
May 31, 2012
Completion
Aug 31, 2012
Last update posted
Dec 22, 2013

2011 – 2012

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Investigator Site Phoenix Arizona
Investigator Site Long Beach California
Investigator Site Newport Beach California
Investigator Site Denver Colorado
Investigator Site Jacksonville Florida
Investigator Site Miami Florida
Investigator Site Miramar Florida
Investigator Site Arlington Heights Illinois
Investigator Site Plainfield Indiana
Investigator Site Henderson Nevada
Investigator Site Hickory North Carolina
Investigator Site High Point North Carolina
Investigator Site Wilmington North Carolina
Investigator Site South Euclid Ohio
Investigator Site Hazleton Pennsylvania
Investigator Site Simpsonville South Carolina
Investigator Site Kingsport Tennessee
Investigator Site Knoxville Tennessee
Investigator Site Nashville Tennessee
Investigator Site San Antonio Texas
Investigator Site Webster Texas
Investigator Site West Jordan Utah

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 NCT01513863, 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 Dec 22, 2013 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01513863 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →