Pilot Study to Evaluate the Somnotouch Device to Quantify Spontaneous Baroreflex Sensitivity

NACompletedINTERVENTIONAL
Enrollment

46

Participants

Timeline

Start Date

December 31, 2015

Primary Completion Date

December 31, 2018

Study Completion Date

December 31, 2018

Conditions
HealthyHeart Failure
Interventions
DEVICE

SOMNOtouch device (Somnomedics)

In each arm, we will evaluate the capacity of SOMNOtouch to measure the baroreflex sensitivity compared to Finapre Nova (reference)

PROCEDURE

Orthostatic test

"For each arm we will proceed to an orthostatic test day one and day two with :~* 10 minutes in supine position~* 10 minutes in sitting position~* 5 minutes in standing position~* 5 minutes in supine position"

DEVICE

Finapres Nova device (FMS system)

Trial Locations (2)

49000

CHU d'Angers, Angers

49325

CH de Cholet, Cholet

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

LivaNova

INDUSTRY

collaborator

SomnoMedics

UNKNOWN

lead

University Hospital, Angers

OTHER_GOV