RecruitingNANCT07514286

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

Sponsor: Rhythm Diagnostic Systems

Trial Details

ConditionAverage Length of Stay, Surgery
InterventionMonitoring by MultiSense
PhaseNA
StatusRecruiting
Participants80
Est. Completion1 Feb 2027
Last Updated17 June 2026

Primary Outcome

The percentage of patients whose care was deemed satisfactory

Eligibility Criteria

Inclusion Criteria

Inclusion Criteria : * 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 Exclusion Criteria : * 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.

Trial Sites

Countries

France
View Registry Entry

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