Imiquimod 5% Cream in Plaque-Type Morphea: A Pilot, Prospective Open-Label Study

This study has been withdrawn prior to enrollment.
(Study never started.)
Sponsor:
Collaborator:
3M
Information provided by:
University of Alberta
ClinicalTrials.gov Identifier:
NCT00230373
First received: September 28, 2005
Last updated: June 17, 2008
Last verified: June 2008

September 28, 2005
June 17, 2008
November 2005
Not Provided
The main outcome of this study is to evaluate the efficacy of imiquimod cream in improving morphea plaques. Improvement of skin induration will be measured by percent improvement in the skin induration as assessed radiologically by ultrasonography score.
Same as current
Complete list of historical versions of study NCT00230373 on ClinicalTrials.gov Archive Site
Any adverse outcome is recorded.
Same as current
Not Provided
Not Provided
 
Imiquimod 5% Cream in Plaque-Type Morphea: A Pilot, Prospective Open-Label Study
Evaluation of the Efficacy and Safety of Imiquimod 5% Cream in Plaque-Type Morphea: A Pilot, Prospective Open-Label Study

Localized scleroderma or morphea is a fibrotic disease, imiquimod induces cytokines which inhibit fibrotic activity . We propose that topical imiquimod 5% cream is efficacious and safe in treating plaque-type morphea. Twenty adults will be enrolled for a pilot study. A screening and baseline clinic visit will be required for each patient enrolled in the study. Each visit will involve completing a medical history, skin examination, digital pictures, histologic examination if the patient consents and an ultrasonographic score. One morphea plaque will be treated with topical imiquimod 5% cream, and another morphea lesion with vehicle cream. Patients will be asked about side effects (local and systemic). Patients will be followed up in the clinic at 3, 6 and 9 months of therapy, and 3 months following end of treatment period (month 12).

Not Provided
Interventional
Phase 3
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Morphea
Drug: imiquimod 5% cream (Aldara)
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
20
June 2007
Not Provided

Inclusion Criteria:

  • Adults and children > 6 years with plaque-type morphea
  • Subject has not participated in previous study involving imiquimod for three months
  • In the investigator's judgement, imiquimod treatment may benefit the patient over conventional treatment
  • Subject has provided informed written consent
  • Female subjects of childbearing potential have a pregnancy urine test that is negative prior to treatment
  • Sexually active subjects agree to practice effective birth control throughout the duration of the study

Exclusion Criteria:

  • Patients with a non-morphea skin disorder in the region of interest
  • Subjects previously undergoing morphea therapy within four weeks of the study
  • Subjects have a known hypersensitivity to imiquimod or component of the cream preparation
  • Subjects who are pregnant or nursing
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00230373
04CA05-IMIQ
Yes
Not Provided
University of Alberta
3M
Principal Investigator: Marlene T Dytoc, MD PhD University of Alberta
University of Alberta
June 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP