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Safety and Performance Study of the MultiSense® Ambulatory Telemonitoring System for Non-critical Patient Management

NCT05357729 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2024-01-05

No results posted yet for this study

Summary

In this clinical investigation, the investigators will assess the safety, performances and clinical added value of the MultiSense® ambulatory telemonitoring solution in real-life situations.

Conditions

  • Visceral and Digestive Surgery
  • Post-surgical Monitoring
  • Post-surgical Rehabilitation

Interventions

DEVICE

MultiSense® remote monitoring

At hospital, the patient will be monitored with conventional monitoring devices as well as the MultiSense® solution (at least one hour with a reference monitor). After hospital discharge, the patients will be remotely monitored by their healthcare professional using the MultiSense® solution.

Sponsors & Collaborators

  • Rhythm Diagnostic Systems

    collaborator INDUSTRY

  • IHU Strasbourg

    lead OTHER

Principal Investigators

  • Michel VIX, MD · Service de Chirurgie Digestive, NHC, HUS

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-14
Primary Completion
2022-09-02
Completion
2022-09-02

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05357729 on ClinicalTrials.gov