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Not Yet RecruitingNCT07514286

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

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Rhythm Diagnostic Systems · Industry
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DEVICEMonitoring by MultiSenseThe MultiSense device will be placed on the patient's back and will allow physicians to remotely monitor six biological parameters

Timeline

Start date
2026-04-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2026-04-07
Last updated
2026-04-07

Locations

4 sites across 1 country: France

Source: ClinicalTrials.gov record NCT07514286. Inclusion in this directory is not an endorsement.

Assessment of the Feasibility and Organisational Impact of a Care Pathway Incorporating the MultiSense® Medical Device f (NCT07514286) · Clinical Trials Directory