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临床试验/NCT04457167
NCT04457167尚未招募不适用

Mastectomy With Retention of the Nipple-areola Complex, Robot-assisted or Not, and / or Immediate or Secondary Reconstruction by Latissimus Dorsi Flap, Robot-assisted or Not.

Institut Paoli-Calmettes2 个研究点 分布在 1 个国家目标入组 480 人开始时间: 2020年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
480
试验地点
2
主要终点
rate of postoperative early complications

研究概览

简要总结

Phase III, non-randomized, monocentric, observational, prospective trial. It is planned to recruit a total of 480 patients, including 240 patients receiving mastectomy with preservation of the nipple-areola complex and 240 patients with a reconstruction with latissimus dorsi flap, or in immediate reconstruction, or during secondary reconstruction.

详细描述

Phase III, non-randomized, monocentric, observational, prospective trial. It is planned to recruit a total of 480 patients, including 240 patients receiving mastectomy with preservation of the nipple-areola complex and 240 patients with a reconstruction with latissimus dorsi flap, or in immediate reconstruction, or during secondary reconstruction.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Age ≥ 18 years old,
  • Signed consent to participate,
  • Women with breast cancer over 18 or at high risk of breast cancer (BRCA 1-2 mutations, PALB2, extensive border lesions)
  • Mastectomy with conservation of the areolo-mammary plaque, or mastectomy without conservation of the areolo-mammary plaque and conservation of the skin case
  • Mastectomy without conservation of the areolo-mammary plate, immediate breast reconstruction by prosthesis,
  • immediate breast reconstruction by autologous latissimus dorsi flap
  • immediate breast reconstruction by latissimus dorsi flap and prosthesis,
  • secondary breast reconstruction by latissimus dorsi flap
  • Affiliation to, or beneficiary of, a social security scheme.

排除标准

  • Patient under 18,
  • Pregnant woman or likely to be (without effective contraception) or breastfeeding,
  • Person in emergency situation, adult person subject to a legal protection measure (adult under guardianship, curatorship or safeguard of justice), or out of state to express his consent,
  • Inability to submit to medical follow-up for the trial for geographic, social or psychological reasons.

结局指标

主要结局

rate of postoperative early complications

时间窗: 90 days

To assess the value of robotic surgery for breast mastectomy with preservation of the nipple-areola complex and immediate or delayed reconstruction by latissimus dorsi flap, with an evaluation of the rate of postoperative early complications (90 postoperative days)

次要结局

未报告次要终点

研究者

发起方
Institut Paoli-Calmettes
申办方类型
Other
责任方
Sponsor

研究点 (2)

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