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临床试验/NCT01696513
NCT01696513已完成不适用

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

Northwestern University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2012年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Change in acne scarring compared to baseline after treatments

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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

研究组 & 干预措施

Subcision & Suction

Experimental

Standard treatment for acne scars followed by suction.

干预措施: Subcision (Procedure)

Subcision

Active Comparator

Standard treatment for acne scars only

干预措施: Subcision (Procedure)

Subcision & Suction

Experimental

Standard treatment for acne scars followed by suction.

干预措施: Suction (Procedure)

结局指标

主要结局

Change in acne scarring compared to baseline after treatments

时间窗: Baseline and 4 months

The change in acne scarring is measured using a global scarring grading system to compare baseline scarring to the treatments.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Murad Alam

Professor in Dermatology, Otolaryngology- Head and Neck Surgery, and Surgery-Organ Transplantation

Northwestern University

研究点 (2)

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Effect of Subcision and Suction on Acne Scars | 临床试验