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A Study to Determine the Safety and Efficacy of Atralin (Tretinoin 0.05%) Gel for the Treatment of Rosacea
This study has been completed.
Sponsored by: Coria Laboratories, Ltd.
Information provided by: Coria Laboratories, Ltd.
ClinicalTrials.gov Identifier: NCT00621218
  Purpose

To compare the efficacy and safety of tretinoin gel 0.05% to its vehicle when dosed once or twice daily in female subjects with rosacea.


Condition Intervention Phase
Rosacea
Drug: tretinoin gel 0.05%
Drug: vehicle
Phase II

MedlinePlus related topics: Rosacea
Drug Information available for: Tretinoin
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Outcomes Assessor), Parallel Assignment, Safety/Efficacy Study
Official Title: A Pilot Study to Compare Tretinoin Gel, 0.05% to Tretinoin Gel Vehicle When Dosed Once or Twice Daily in Female Subjects With Classical Rosacea

Further study details as provided by Coria Laboratories, Ltd.:

Primary Outcome Measures:
  • Improvement in signs and symptoms of rosacea [ Time Frame: 16 weeks ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Changes in various skin parameters [ Time Frame: 16 weeks ] [ Designated as safety issue: Yes ]

Enrollment: 36
Study Start Date: February 2008
Study Completion Date: December 2008
Primary Completion Date: April 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Active Comparator Drug: tretinoin gel 0.05%
Apply tretinoin gel, 0.05% topically once or twice daily to female subjects with rosacea
2: Placebo Comparator Drug: vehicle
Apply Atralin Gel vehicle topically once or twice daily to female subjects with rosacea.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Female
  • Age 18-65
  • Diagnosed with classical, centrofacial, erythemato-telangiectatic rosacea

Exclusion Criteria:

  • Male, females less than 18 years
  • Females over 65 years
  • No diagnosed rosacea
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00621218

Locations
United States, Pennsylvania
Product Investigations, Inc.
Conshohocken, Pennsylvania, United States, 19428
Sponsors and Collaborators
Coria Laboratories, Ltd.
Investigators
Principal Investigator: Morris V Shelanski, MD Unaffiliated
  More Information

Responsible Party: Coria Laboratories, Ltd. ( D. Innes Cargill, PhD )
Study ID Numbers: 9320-010-002
Study First Received: February 12, 2008
Last Updated: December 17, 2008
ClinicalTrials.gov Identifier: NCT00621218  
Health Authority: United States: Institutional Review Board;   United States: Food and Drug Administration

Keywords provided by Coria Laboratories, Ltd.:
tretinoin, efficacy, safety, rosacea

Study placed in the following topic categories:
Rosacea
Skin Diseases
Tretinoin

Additional relevant MeSH terms:
Keratolytic Agents
Antineoplastic Agents
Therapeutic Uses
Dermatologic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009