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临床试验/NCT04688697
NCT04688697进行中(未招募)不适用

A Multicentric, Open-labeled, Prospective, Randomized Controlled Study to Compare the Satisfaction and Safety of the Prepectoral and Subpectoral Implant-based Breast Reconstruction in Patients Receiving Immediate Breast Reconstruction Using Implant Combined With TiLoop® Bra After Skin Sparing or Nipple-areola Sparing Mastectomy

Fudan University1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年5月12日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
300
试验地点
1
主要终点
Patients' satisfaction

研究概览

简要总结

Breast cancer is one of the main malignant tumors threatening women's lives. In recent years, the increasing demand for reconstruction of breast cancer patients in China has made the proportion of breast reconstruction increase year by year, while implant reconstruction has become the most important way of breast reconstruction due to its less injury, shorter time of operation and relatively simple surgical technique. In the long-term clinical practice, due to the lack of safe and effective alternative methods, the reconstruction method with prosthesis placed to posterior pectoralis major has been accepted by surgeons and patients, and has become the most commonly used method of prosthesis construction. However, the development of biomaterials provides new ideas for breast reconstruction. At present, more and more doctors in clinical practice discontinue the use of serratus anterior, but use the synthetic mesh (mostly titanium mesh TiLoop® Bra) or allogeneic acellular dermal matrix mesh to cover part of the dilator or prosthesis so as to shorten the entire operation cycle and make the appearance of the reconstructed breast more natural and aesthetic. In particular, it can improve the contour of the folds under the breast and shape the breasts with a certain degree of sagging.

This study takes the patients receiving immediate reconstruction with an implant combined with TiLoop® Bra after total mastectomy as the subjects, aiming to compare the aesthetics and safety of the placement of implant to anterior and posterior pectoralis major through a prospective and randomized study. The primary objective of the study is to analyze the aesthetics of breast appearance, patient satisfaction and postoperative quality of life (QOL) of the placement of implant to anterior and posterior pectoralis major. The secondary objective of the study is to analyze the incidence of complications and type of reoperation in both groups.

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 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • More than 18 years old
  • Preoperative pathology confirming invasive breast carcinoma or ductal carcinoma in situ
  • Clinical T1 and T2 (Maximum tumor diameter ≤5 cm)
  • Clinical ALN negative (Clinical physical examination and ultrasound indicate axillary lymph node negative; Suspected abnormality of axillary lymph node, and fine needle aspiration negative)
  • No clinical or imaging evidence of distant metastasis
  • Patients to receive skin sparing mastectomy or nipple sparing mastectomy
  • Patients with no or mild mastoptosis
  • Prosthesis to be implanted <500 ml
  • Be able and willing to sign the Informed Consent Form (ICF)

排除标准

  • Patients with the breast of moderate-severe mastoptosis, or requiring the use of Wise-pattern or other breast lift methods for subcutaneous mammary gland resection
  • Patients who have received symmetrical breast surgery on the unaffected side immediately or later
  • Patients with locally advanced breast cancer to receive neoadjuvant therapy
  • Patients currently participating in other clinical trials, which may have impact on the participation in this trial
  • Neoadjuvant therapy has been completed, and there is clear indication of adjuvant radiotherapy after the operation
  • Previous history of breast cancer (patients with ipsilateral recurrence after breast sparing surgery)
  • Pregnancy breast-feeding women
  • History of smoking
  • Previous history of diabetes

结局指标

主要结局

Patients' satisfaction

时间窗: 18 months after the operation

Patients' satisfaction evaluated based on Breast-Q scale

次要结局

  • Incidences of complications and serious complications(During 18 months after the operation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jiong Wu

Professor, Vise President

Fudan University

研究点 (1)

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