LONG PULSED ND:YAG LASER (1064 NM) VERSUS INTENSE PULSED LIGHT IN TREATMENT OF TRAUMATIC AND POST-SURGICAL ERYTHEMATOUS SCARS

Alexandria University1 个研究点分布在 1 个国家目标入组 40 人开始时间: 2022年11月16日最近更新: 2026年5月20日

试验速览

阶段: 不适用
状态: 已完成
发起方: Alexandria University
入组人数: 40
试验地点: 1

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

The goal of this clinical trial is to compare the efficacy and safety of long-pulsed ND:YAG laser and intense pulsed light in the treatment of traumatic and post-surgical erythematous scars. Forty patients presenting with traumatic and post-surgical erythematous scars on the head and neck, of six months' duration or less, were randomly divided into two equal groups. Group A patients received long-pulsed ND:YAG laser sessions, while Group B patients received intense pulsed light sessions. Four sessions were given at four-week intervals.

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: 12 Years 至 —（Child, Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Patients of either gender, aged more than 12 years, presenting with an erythematous scar on the head and neck area, traumatic or post-surgical, and of a duration equal to or less than six months.

排除标准

•1. Patients with post burn scars, scars of more than six months duration, keloids, post acne atrophic erythematous scars or scars that are not located on the head and neck area.
•2. Patients with active bacterial, viral, or fungal cutaneous infection within the scar tissue.
•3. Patients who are pregnant or lactating.
•Known contraindication to laser therapy.
•Use of Isotretinoin within the previous 6 months.

研究者

发起方

Alexandria University

申办方类型

Other

责任方

Sponsor

研究点 (1)

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