Assessment of the Feasibility and Organisational Impact of a Care Pathway Incorporating the MultiSense® Medical Device for Post-operative Home Monitoring of Elderly Patients.
Recruiting now · Not applicable
Conditions studied: Average Length of Stay, Surgery
In brief
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.
Key facts
- Study ID
- NCT07514286
- Run by
- Rhythm Diagnostic Systems
- People needed
- 80
- Starts
- 2026-06-03
- Expected to finish
- 2027-02-01
- Last updated by the study team
- 2026-06-17
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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.
Where it is running
- Western Cancer Institute of Nantes — Nantes, France (enrolling)
- Western Cancer Institute of Angers — Angers, France
- Bergonié Insititute — Bordeaux, France
- Inter-municipal Hospital Centre of Mont-de-marsan — Mont-de-Marsan, France
Full record on ClinicalTrials.gov
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