跳至主要内容
临床试验/NCT06744998
NCT06744998尚未招募不适用

Hemopatch Implication After Axillary Dissection for Breast Cancer: a Randomized Clinical Study

European Institute of Oncology2 个研究点 分布在 1 个国家目标入组 190 人开始时间: 2025年2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
190
试验地点
2
主要终点
Axillary seroma evaluation

研究概览

简要总结

Aim of this randomized study is to assess the value of a different haemostatic sealant, the Hemopatch®, in axillary lymph node dissection (ALND) to reduce the incidence of seroma and seroma-related complications.

详细描述

With the de-escalation of axillary lymph node dissection (ALND) to sentinel lymph node biopsy as a surgical procedure staging in breast cancer (BC), the physical and psychological morbidity has been improved significantly. However, ALND is still considered in a relevant number of BC patients as treatment for controlling locoregional axillary disease, and these patients present still important complications related to ALND, such as neuropathy, limitation of shoulder movement, arm lymphedema, and most commonly seroma evolution.

Multiple surgical devices with the intent to improve sealing of lymphatic and blood vessels have demonstrated contrasting results in the incidence of seroma formation after ALND and are no utilized routinary. Non-surgical devices, such as chemical medications, sealing small vessels by stimulating collagen and fibrinogen syntheses, also could improve to sealing of the lymphatic vessels. Additionally, fibrin glue-coated collagen patches and fibrin glue application to the surgical cavity were already tested in ALND patients with contrasting benefit in term of seroma prevention. Unfortunately, none of these studies provided a good solution to eliminate or reduce the incidence of seroma after ALND in BC treatment.

Aim of this randomized study is to assess the value of a different haemostatic sealant, the Hemopatch®, in axillary lymph node dissection (ALND) to reduce the incidence of seroma and seroma-related complications.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with primary breast cancer
  • Mastectomy or breast conserving surgery
  • Patients eligible for axillary dissection
  • Male or female
  • Previous (or not) neoadjuvant treatments
  • Any breast histotypes

排除标准

  • Previous axillary surgery

结局指标

主要结局

Axillary seroma evaluation

时间窗: 1 week

Measure of drain output (in cc) in one week

次要结局

  • Hospital access evaluation(1 month)
  • Drain duration evaluation(1 month)

研究者

发起方
European Institute of Oncology
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验