NL-OMON55074已完成不适用
The effect of microneedling on abdominal scarring after DIEP flap breast reconstruction - MARS-trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64（—）
入选标准
- •- Have an abdominal scar resulting from a DIEP flap breast reconstruction in
- •the past 18 months, but at least 3 months ago;
- •- Have a wish for improvement on pain, itching, color, stiffness, thickness,
- •irregularity or overall scar quality with regard to the abdominal scar;
- •- Age equal of above 18 years;
- •- Dutch or English speaking, reading and writing;
- •- Is able to provide informed consent IC;
- •- Fitzpatrick type I-III
排除标准
- •- Are currently applying or receiving any form of scar therapy what needs to be
- •continued during the study;
- •- Have permanent filler injections in the abdominal scar;
- •- Have the desire to undergo scar reconstruction surgery during the study;
- •- Are on chemotherapy or radiotherapy;
- •- Have a presence of skin cancers, warts, solar keratosis, or any skin
- •infection in the abdominal scar area;
- •- Have keloid scarring in the abdominal scar area or the tendency to develop
- •keloid scarring based on previous developed keloid scars;
- •- Are not willing to use sun protecting factor (SPF) for the period of 4 weeks
- •after each microneedling session;
- •- Have an uncontrollable coagulation status;
- •- Are or become palliative or terminal;
- •- Have or develop a serious systemic disease;
- •- Are pregnant or have the wish to become pregnant during the study;
- •- Who are simultaneous participate in another scientific study interfering with
- •the abdominal scar formation.
研究者
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