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临床试验/NCT05888571
NCT05888571招募中不适用

A Randomized Controlled Trial of Prepectoral Breast Reconstruction With and Without Mesh

Tianjin Medical University Cancer Institute and Hospital1 个研究点 分布在 1 个国家目标入组 164 人开始时间: 2023年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
164
试验地点
1
主要终点
Major Complication Rates

研究概览

简要总结

To explore the efficacy and safety that occur after immediate prepectoral breast reconstruction when TiLOOP Mesh is used compared to that when TiLOOP Mesh is not used.

详细描述

The clinical study aims to explore the efficacy and safety that occur after immediate prepectoral breast reconstruction when TiLOOP Mesh is used compared to that not using TiLOOP Mesh.

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
None

入排标准

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

入选标准

  • Adult women aged 18-65 years who plan to undergo unilateral or bilateral immediate prepectoral prothesis breast reconstruction;
  • SSM or NSM or Skin-Reducing Mastectomy for breast cancer patients or prophylactic mastectomy;
  • Tissue expander size =<800cc, implant size =<600cc;
  • The blood perfusion of breast skin flap was well;
  • Do not smoking in the last 4 weeks or more
  • Patients with normal expectations and mental health for breast reconstruction;
  • Signed consent to participate

排除标准

  • Poor perfusion of breast mastectomy flap;
  • II stage breast reconstruction patients;
  • History of chest radiotherapy;
  • BMI greater than 35;
  • Patients who have not quit smoking within the last 4 weeks;

结局指标

主要结局

Major Complication Rates

时间窗: up to 12 months after surgery

The rate of major complications in the two groups

Patient Breast-Q questionnaire

时间窗: up to 12 months after surgery

We use the Breast-Q questionnaire to evaluate patients' satisfaction via the reconstruction module of BREAST-Q.

次要结局

  • Minor Complication Rates(up to 12 months after surgery)
  • The rate of surgical revision of reconstructed breasts(up to 12 months after surgery)
  • Rates of capsule contracture(up to 24 months after surgery)
  • The rate of implant or tissue expander removal(up to 12 months after surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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