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NCT01696513 Clinical Trial

Effect of Subcision and Suction on Acne Scars

Acne Scars Clinical Trial

Official title:
Pilot Split Face Randomized, Evaluator Blinded Study on the Effect of Subcision and Suctioning With a Microdermabrasion Device on Rolling Acne Scars

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT01696513
Other study ID # STU66710
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 2012
Est. completion date December 2024

Study information
Verified date January 2024
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 20
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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 Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Suction

• Subcision

Locations
Country Name City State
United States Northwestern University Feinberg School of Medicine, Department of Dermatology Chicago Illinois

Sponsors (1)
Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in acne scarring compared to baseline after treatments The change in acne scarring is measured using a global scarring grading system to compare baseline scarring to the treatments. Baseline and 4 months
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