- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01696513
Effect of Subcision and Suction on Acne Scars
January 29, 2025 updated by: Murad Alam, Northwestern University
Pilot Split Face Randomized, Evaluator Blinded Study on the Effect of Subcision and Suctioning with a Microdermabrasion Device on Rolling Acne Scars
The primary objective of this study is to determine whether the use of standard treatment in conjunction with suction will improve acne scars compared to a standard treatment alone.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60611
- Northwestern University Feinberg School of Medicine, Department of Dermatology
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age 18 and over
- Have bilateral rolling acne scars
- Are in good health
- Subject has the willingness and ability to understand and provide informed consent for the use of their tissue and communicate with the investigator.
Exclusion Criteria:
- Under 18 years of age
- Pregnancy or lactation
- Unable to understand the protocol or give informed consent
- Has mental illness
- Recent Accutane use in the past 6 months
- Prone to hypertrophic and keloidal scarring
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Subcision & Suction
Standard treatment for acne scars followed by suction.
|
|
|
Active Comparator: Subcision
Standard treatment for acne scars only
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in acne scarring compared to baseline after treatments
Time Frame: Baseline and 4 months
|
The change in acne scarring is measured using a global scarring grading system to compare baseline scarring to the treatments.
|
Baseline and 4 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Murad Alam, MD, Northwestern University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2012
Primary Completion (Estimated)
December 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
September 14, 2012
First Submitted That Met QC Criteria
September 27, 2012
First Posted (Estimated)
October 1, 2012
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 29, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STU66710
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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