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A Multi-Center Study of Short and Long-term Use of Protopic Ointment in Patients with Atopic Dermatitis - Article


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Erythromycin Ophthalmic Ointment

Ilotycin



Clinical Trial: A Multi-Center Study of Short and Long-term Use of Protopic Ointment in Patients with Atopic Dermatitis

This study is currently recruiting patients.

Sponsored by: Astellas Pharma US, Inc.
Information provided by: Astellas Pharma US, Inc.

Purpose

The purpose of the study is to determine the impact of topical corticosteroids on the safety and effectiveness of Protopic Ointment in the short-term treatment of moderate to severe Atopic Dermatitis and to compare the safety and effectiveness of Protopic Ointment and vehicle (ointment base without the active drug) in the long-term management of Atopic Dermatitis.

Condition Treatment or Intervention Phase
Dermatitis, Atopic
 Drug: topical tacrolimus (Protopic Ointment)
Phase IV

MedlinePlus related topics:  Allergy;   Dermatitis;   Genetic Disorders;   Skin Diseases

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: A Multi-Center Study to Assess the Impact of Topical Corticosteroids on the Safety and Efficacy of Protopic Ointment in the Short-Term Treatment of Atopic Dermatitis and to Assess Protopic in the Long-term Management of Atopic Dermatitis

Further Study Details: 
Primary Outcomes: The primary outcome is the percentage of patients reporting cutaneous adverse events during the first 2 weeks of treatment
Secondary Outcomes: The secondary outcome is the percentage of patients reporting cutaneous adverse events overall
Expected Total Enrollment:  400

Study start: October 2004;  Expected completion: April 2007
Last follow-up: April 2006;  Data entry closure: October 2006

Eligibility

Ages Eligible for Study:  2 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Patient must have Atopic Dermatitis
  • Patient must be at least 2 years of age

Exclusion Criteria:

  • Patient is pregnant or breast feeding an infant

Location and Contact Information

Medical Information      800-727-7003    medical_information@fujisawa.com

Alabama
      Investigational Site, Birmingham,  Alabama,  35205,  United States; Recruiting

California
      Investigational Site, Irvine,  California,  92697,  United States; Recruiting

      Investigational Site, San Diego,  California,  92123,  United States; Recruiting

      Investigational Site, Loma Linda,  California,  92354,  United States; Recruiting

Georgia
      Investigational Site, Atlanta,  Georgia,  30322,  United States; Recruiting

Illinois
      Investigational Site, Chicago,  Illinois,  60611,  United States; Recruiting

      Investigational Site, Chicago,  Illinois,  60614,  United States; Recruiting

Michigan
      Investigational Site, Ann Arbor,  Michigan,  48109,  United States; Recruiting

      Investigational Site, Detroit,  Michigan,  48202,  United States; Recruiting

Missouri
      Investigational Site, St. Louis,  Missouri,  63110,  United States; Recruiting

New Hampshire
      Investigational Site, Lebanon,  New Hampshire,  03756,  United States; Recruiting

New York
      Investigational Site, New York,  New York,  10029,  United States; Recruiting

North Carolina
      Investigational Site, Winston Salem,  North Carolina,  27157,  United States; Recruiting

Ohio
      Investigational Site, Cincinnati,  Ohio,  45219,  United States; Recruiting

Oregon
      Investigational Site, Portland,  Oregon,  97201,  United States; Recruiting

Pennsylvania
      Investigational Site, Philadelphia,  Pennsylvania,  19115,  United States; Recruiting

Tennessee
      Investigational Site, Nashville,  Tennessee,  37215,  United States; Recruiting

Texas
      Investigational Site, Dallas,  Texas,  75390,  United States; Recruiting

      Investigational Site, Dallas,  Texas,  75230,  United States; Recruiting

More Information

Study ID Numbers:  20-04-002
Record last reviewed:  March 2005
Last Updated:  March 28, 2005
Record first received:  March 25, 2005
ClinicalTrials.gov Identifier:  NCT00106496
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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Page Updated: June 1, 2005
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