跳至主要内容
临床试验/NCT07514286
NCT07514286招募中不适用

Assessment of the Feasibility and Organisational Impact of a Care Pathway Incorporating the MultiSense® Medical Device for Post-operative Home Monitoring of Elderly Patients.

Rhythm Diagnostic Systems4 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年6月3日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
80
试验地点
4

研究概览

简要总结

Assessing the clinical and organisational impact of a home-based post-operative monitoring strategy incorporating the MultiSense® device involving 80 patients aged 65 years and over who have undergone major surgery.

详细描述

Evaluate the clinical and organisational impact of a post-operative home monitoring strategy incorporating the MultiSense® device in elderly patients.

The study will be conducted in a multicentre setting, involving 80 patients aged 65 years and over who have undergone major surgery.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient aged 65 or over
  • Patient eligible for remote monitoring using the MultiSense® device
  • No psychiatric illness that would prevent them from giving informed consent or receiving optimal treatment and follow-up care
  • Subject affiliated with a health insurance scheme
  • Subject able to read and understand English
  • Subject who has signed an informed consent form
  • Subjects indicated for scheduled surgery
  • Patients indicated for scheduled surgery :
  • Transverse colectomy, by laparotomy
  • Hepatic laparoscopy
  • Laparoscopic or laparoscopic liver surgery (code hlfc or hlfa for procedures)
  • Hysterectomy
  • Adnexectomy
  • Parietal surgery (eventration)
  • Rectal resection
  • Right and left colectomy
  • Stoma closure by direct approach

排除标准

  • Patients already participating in an interventional clinical trial.
  • Patients subject to legal protection measures, guardianship, curatorship, or deprived of their liberty by judicial or administrative decision.
  • Patients hospitalised without consent.
  • Patients unable to complete a questionnaire and without a close relative to assist them in using the solution.
  • Patients admitted to or residing in a health or social care facility (other than for the surgery itself).
  • Persons admitted to or residing in a health or social care institution (other than for the surgery itself);
  • Persons unable to give their free and informed consent.

研究者

发起方
Rhythm Diagnostic Systems
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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