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The primary objective of this study is to determine the efficacy of a needling device for treatment of acne scars.
We are investigating a needled micro-roller for use in improving the appearance of acne scars. The study is being conducted under the direction of Dr. Murad Alam of Northwestern University, Department of Dermatology.
The needles on the micro-roller are designed to create small holes in the top and mid layers of skin in order to induce the formation of more collagen, which would in turn help improve the appearance of acne scars. To qualify for the study, you must have at least 2 large areas of the face with acne scars.
The study is designed such that one part of your face, which has acne scars, will be treated with the device on 3 separate occasions, spaced 2 weeks apart at our clinic in Chicago at Northwestern. We would also ask you to return at 3 months and at 6 months to have photographs taken.
If you are interested in participating, we would like to get you involved as soon as possible
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| needling treatment | Experimental | Needling treatment applied to half of the face at each study visit |
|
| Control | No Intervention | No treatment applied to half of the face |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| needling treatment | Procedure | Needling treatment applied to half of the face at each study visit |
|
| Measure | Description | Time Frame |
|---|---|---|
| We will evaluate qualitatively and quantitatively the improvement of the subject's acne scars | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| The tolerability of the treatment will be assessed | 4 weeks | |
| Subject satisfaction will be determined | 6 months | |
| Any adverse events of this treatment will be recorded. |
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Inclusion Criteria:
Exclusion Criteria:
Pregnancy and lactation
Subjects with history of keloid or hypertrophic scars
Subjects with active skin disease (other than mild acne) or skin infection in the treatment area
Subjects with an active systematic or local skin disease that is likely to alter wound healing
Subjects who have undergone in the past 6 months or planning to undergo in the next 6 months the following cosmetic treatments in the acne scar area
Subjects taking the following prescription medications:
Subjects who allergic to lidocaine and prilocaine
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| Name | Affiliation | Role |
|---|---|---|
| Murad Alam, MD | Northwestern University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Northwestern University Feinberg School of Medicine, Department of Dermatology | Chicago | Illinois | 60611 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 24919799 | Derived | Alam M, Han S, Pongprutthipan M, Disphanurat W, Kakar R, Nodzenski M, Pace N, Kim N, Yoo S, Veledar E, Poon E, West DP. Efficacy of a needling device for the treatment of acne scars: a randomized clinical trial. JAMA Dermatol. 2014 Aug;150(8):844-9. doi: 10.1001/jamadermatol.2013.8687. |
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| 6 months |