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临床试验/NCT07236359
NCT07236359尚未招募不适用

A Randomised Control Trial Evaluating Well Being and Patient Reported Outcomes After Robotic Single-port Nipple Sparing Mastectomy and Implant Reconstruction

Beaumont Hospital0 个研究点目标入组 108 人开始时间: 2025年12月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
108
主要终点
Primary Outcome Measure

研究概览

简要总结

This study is being carried out to better understand how different types of mastectomy surgeries affect women's recovery, satisfaction, and overall well-being after breast cancer surgery and reconstruction. There are different ways to perform a mastectomy. In some patients, a nipple-sparing mastectomy may be suitable, where the nipple and surrounding breast skin are preserved. This approach allows for immediate breast reconstruction with an implant, which is placed at the same time as the mastectomy to restore the breast shape. A newer technique called robotic single-port nipple-sparing mastectomy uses advanced robotic technology to remove breast tissue through a small hidden incision at the side of the chest. This method may reduce scarring, pain, and recovery time, while preserving the appearance and sensation of the breast.

However, while early studies suggest this technique is safe and effective, more evidence is needed to compare it directly with standard surgeries.

This study will compare:

  • Robotic nipple-sparing mastectomy
  • Standard (open) nipple-sparing mastectomy We will assess patient satisfaction, body image, physical and emotional well-being, and surgical outcomes over 12 months following surgery. By taking part, you are helping researchers evaluate whether robotic and nipple-sparing approaches offer measurable benefits to patients.

Taking part in this study will not affect your surgery or the care you receive. You will be given the best treatment available based on your individual medical needs, whether or not you decide to participate in the research.

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

入选标准

  • •Women aged 18 years and older
  • •Candidates who have already been selected to undergo nipple sparing mastectomy and immediate implant reconstruction by the breast MDT for the following indications:
  • •Genetic mutation carriers undergoing risk-reducing mastectomy.
  • •Ductal carcinoma in situ (DCIS) requiring mastectomy.
  • •Early invasive breast cancer requiring mastectomy.
  • •The tumour must not have skin involvement and no evidence of invasive disease within 1cm of skin, nipple or Pec major muscle (as proven on MRI).
  • •Candidates for immediate breast reconstruction with IMPLANT reconstruction
  • •Fluent in English
  • •Fit for general anaesthetic
  • •Signed informed consent form

排除标准

  • •Advanced breast cancer with skin involvement.
  • •Nipple involvement for Nipple Sparing Mastectomy Arms.
  • •Prior chest wall radiation therapy
  • •Pregnancy
  • •Lactation
  • •Patients with insufficient English to sign an informed consent (i.e. interpreter required).

研究组 & 干预措施

Single-port robotic nipple-sparing mastectomy with immediately implant based reconstruction.

Experimental

Intervention

干预措施: Intervention (Procedure)

Standard open nipple sparing mastectomy with immediate implant-based reconstruction.

Active Comparator

Standard of care

干预措施: Standard open nipple sparing mastectomy with immediate implant-based reconstruction (Procedure)

结局指标

主要结局

Primary Outcome Measure

时间窗: 1 year

The primary endpoint of this study is the difference Breast Q scores at 12 months.

Secondary Outcome Measures

时间窗: 1 year

* Surgical complication rates within 30 and 90 days, classified according to the Clavien-Dindo system. * Reoperation rates and need for unplanned return to theatre. * Length of hospital stay and drain duration * Operative time and estimated intraoperative blood loss. * Time to return to daily activities including work and physical exercise. * Aesthetic outcomes, assessed both by patient-reported satisfaction and by an independent panel review of standardized postoperative photographs. * Oncologic outcomes, including final pathology margin status and local recurrence (if applicable during follow-up). * Amount of residual breast tissue left on post operative MRI at 6 months in the different groups.

次要结局

未报告次要终点

研究者

发起方
Beaumont Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Arnold Hill

Professor

Beaumont Hospital

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