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Evaluation of RDS MultiSense® in Desaturation Analysis in Healthy Volunteers

NCT05044585 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2023-02-28

No results posted yet for this study

Summary

In this clinical study, the investigators will compare vital parameters measurements obtained using continuous data from reference monitors and continuous wireless MultiSense® monitoring patch in 30 healthy volunteers under induced and controlled hypoxia.

Conditions

Interventions

OTHER

Remote Automated Monitoring System

The subject will be monitored with conventional monitoring devices as well as the MultiSense patch.

Sponsors & Collaborators

  • Rhythm Diagnostic Systems

    collaborator INDUSTRY

  • IHU Strasbourg

    lead OTHER

Principal Investigators

  • Bernard Geny, Pr · Physiology and Functional Exploration, NHC Strasbourg, France

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-13
Primary Completion
2022-09-13
Completion
2022-09-13

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT05044585 on ClinicalTrials.gov