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临床试验/NL-OMON28278
NL-OMON28278已完成不适用

The effect of microneedling on abdominal scarring after DIEP flap breast reconstruction

Radboudumc and University of Applied Sciences Utrecht0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
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

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 of (at least 10 cm) the abdominal scar;
  • - Age equal or above 18 years;
  • - Dutch speaking, reading and writing;
  • - Able to provide informed consent;
  • - Fitzpatrick type I-III according to the classification of skin phototype (I-IV).

排除标准

  • - Are currently applying or receiving any form of scar therapy what needs to be continued during the study;
  • - Consider 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 or become pregnant or have a wish to become pregnant during the study;
  • - Who are simultaneous participate in another scientific study interfering with the abdominal scar formation.

研究者

发起方
Radboudumc and University of Applied Sciences Utrecht

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