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 N/A Interventional Study
Average Length of Stay Surgery
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
65 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
80 (estimated)
Sponsor
Rhythm Diagnostic Systems · Industry
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About This Trial

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.

Trial Locations
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Eligibility 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 * …
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