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临床试验/NCT07006662
NCT07006662招募中不适用

Anatomical Landmarks for Chest Wall Perforators Used for Partial Breast Reconstruction (LaPBrecon)

University Hospitals of North Midlands NHS Trust2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2026年8月4日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
2
主要终点
Location of vesselse

研究概览

简要总结

The aim of this 6-month proof-of-concept study is to map out the chest wall perforators in relation to anatomical landmarks for partial breast reconstruction.

详细描述

Breast conserving surgery is commonly performed in patients with breast cancer. It is important to fill the defect from a breast conserving procedure to achieve good cosmetic outcome. This defect can be filled either by using the adjacent breast tissue or by using perforator flaps; commonly taken from the area posterolateral to the breast or or below the inframammary crease. These perforator flaps can be based on thoracodorsal artery, lateral thoracic artery, lateral intercostal artery or the medial intercostal artery. The identification of these perforators using a hand-held doppler is an important but time-consuming intraoperative step. Surgeons often use the information derived from cadaveric studies when identifying these perforators as there is minimal information on the location of these perforators in relation to anatomical landmarks.

Patients with a BMI of < 25 Kg/m2admitted for elective breast surgery or attending breast outpatients' clinic will be included in the study. Patients will be sent information about this study prior to admission or the clinic appointment with a copy of the consent form. Participants will have a 30-minute assessment using a hand held doppler and perforators will be mapped against soft tissue and bony landmarks. Data will be analysed to identify common anatomical locations for the different chest wall perforators.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

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

  • Patients undergoing elective breast surgery
  • Age ≥ 18 years
  • BMI ≤ 30 kg/m2
  • Willing and able to give fully informed consent,
  • Willing and able to comply with the study procedures

排除标准

  • Pregnant patients
  • Previous bilateral Breast or axillary surgery
  • Undergoing bilateral oncoplastic procedure or requiring bilateral pre-operative marking
  • Undergoing breast surgery requiring pre-operative marking of some of the landmarks and has had contralateral breast or axillary surgery in the past
  • Surgery planned within 24 hours of screening for eligibility
  • Known history of allergy or contact dermatitis to ultrasound gels

结局指标

主要结局

Location of vesselse

时间窗: 6 months

The location of the AICAP vessels in vertical and horizontal axis using constant bony and soft tissue landmarks. This will be measured by the distance of the perforators from the anatomical landmarks

Location of vessels

时间窗: 6 months

The location of the MICAP vessels in vertical and horizontal axis using constant bony and soft tissue landmarks. This will be measured by the distance of the perforators from the anatomical landmarks

次要结局

  • Variability(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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