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Imiquimod 5% Cream in Plaque-type Morphea: A Pilot, Prospective Open-label Study

Primary Purpose

Morphea

Status
Withdrawn
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
imiquimod 5% cream (Aldara)
Sponsored by
University of Alberta
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Morphea focused on measuring Localized scleroderma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Dr. Marlene Dytoc's clinic
  • University of Alberta
  • Dr. Loretta Fiorillo's clinic

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Any adverse outcome is recorded.

Full Information

First Posted
September 28, 2005
Last Updated
April 22, 2015
Sponsor
University of Alberta
Collaborators
3M
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1. Study Identification

Unique Protocol Identification Number
NCT00230373
Brief Title
Imiquimod 5% Cream in Plaque-type Morphea: A Pilot, Prospective Open-label Study
Official Title
Evaluation of the Efficacy and Safety of Imiquimod 5% Cream in Plaque-type Morphea: A Pilot, Prospective Open-label Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Withdrawn
Why Stopped
Study never started.
Study Start Date
November 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2007 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Alberta
Collaborators
3M

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morphea
Keywords
Localized scleroderma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
imiquimod 5% cream (Aldara)
Primary Outcome Measure Information:
Title
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.
Secondary Outcome Measure Information:
Title
Any adverse outcome is recorded.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marlene T Dytoc, MD PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr. Marlene Dytoc's clinic
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2C8
Country
Canada
Facility Name
University of Alberta
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2G3
Country
Canada
Facility Name
Dr. Loretta Fiorillo's clinic
City
Red Deer
State/Province
Alberta
ZIP/Postal Code
T4N 6R2
Country
Canada

12. IPD Sharing Statement

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Imiquimod 5% Cream in Plaque-type Morphea: A Pilot, Prospective Open-label Study

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