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临床试验/NCT06749561
NCT06749561进行中(未招募)不适用

A Comparative Investigation of Efficacy and Complications in Light and Deep Chemical Peels

Superior University1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
112
试验地点
1
主要终点
Dermatological Assessment Score (DAS)

研究概览

简要总结

Chemical peeling involves applying substances to the skin to induce controlled damage, which promotes the regeneration of fresh skin cells and enhances the skin's appearance.

详细描述

This study will be a cross-sectional analysis with a sample size of 112 patients.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Healthy males and females aged 18-35 years.
  • Willing to provide informed consent and follow the treatment protocol.

排除标准

  • Pregnant or breastfeeding women.
  • Active skin conditions (e.g., acne, eczema).
  • Use of medications that affect skin healing.
  • Known allergies to chemical peel substances.

结局指标

主要结局

Dermatological Assessment Score (DAS)

时间窗: 12 Months

The area-wise percentage involvement of the involved sites is calculated as: 1 = less than 10% area; 2 = 10-29%; 3 = 30-49%; 4 = 50-69%; 5 = 70-89%; and 6 = more than 90%. The maximum score of PASI is 72. PASI 75 is a 75% reduction of baseline PASI score.

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

Muhammad Naveed Babur

Principal Investigator

Superior University

研究点 (1)

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