跳至主要内容
临床试验/ACTRN12624000183583
ACTRN12624000183583尚未招募Unknown

A prospective study of deep inferior epigastric perforator (DIEP) flap viability assessment and monitoring using continuous visible light spectroscopy: A Pilot Study in women undergoing DIEP flap reconstruction procedure.

Chris O'Brien Lifehouse0 个研究点目标入组 15 人开始时间: 2024年2月26日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Female

入选标准

  • 1. Patient older than 18 years of age (no upper age limit)
  • 2. Is about to undergo a DIEP flap reconstruction procedure (unilateral / bilateral) after diagnosis and treatment of breast cancer
  • 3. Willing to provide consent and participate in the study, complying to all study requirements
  • 4. Patients in the learning curve”
  • learning curve group is defined as the group of first few participants using the T-stat device. As the research team is using this new device for the first time and are adjusting to the usage of this device, results of these learning curve group may not be the optimal, but we are still including them in this study as this is a pilot study with a small sample size to test the feasibility of the device and looking at the possibility of expanding into a future large trial with a greater pool of patients.

排除标准

  • 1.Patients who are unable to read and write in English to a level required for consent and completion of questionnaires.
  • 2.Patient who are or potentially may be allergic to the T-stat device sensor patch.
  • 3.Patients whose skin, due to a named or unnamed condition, presents with non-clear fluid production that may interfere with the light signal.
  • 4.Patients who have an existing sleep disorder (e.g sleep apnoea, insomnia, parasomnias, restless leg syndrome) which can interfere with their judgement of their post-operative sleep quality.
  • 5.Patients who have an existing mental disorder (e.g depression, anxiety) which may interfere with their ability to provide accurate responses to the SF-36 and Breast Q questionnaires.

研究者

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