Laboratoire TIMC
Grenoble, 38000, France
Location contact
Julie Fontecave
CONTACT
Julie Fontecave
SUB_INVESTIGATOR
Nicolas Segond
SUB_INVESTIGATOR
Stéphane TANGUY
CONTACT
NCT Number: NCT06742775
Acquisition of synchronized cardiovascular signals from non-invasive measurements (ECG, photoplethysmography pulse sensors, inductance plethysmography) in healthy volunteers aged from 18 to 75, during spontaneous ventilation with apneas (20 seconds) for a total acquisition time of 30 minutes.
Trial opening soon.
Get Notified18 year–75 year
All sexes
Observational
Grenoble, 38000, France
Julie Fontecave
CONTACT
Julie Fontecave
SUB_INVESTIGATOR
Nicolas Segond
SUB_INVESTIGATOR
Stéphane TANGUY
CONTACT
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects will be fitted with non-intrusive devices. In a semi-recumbent position, they will be asked to perform
This single participation session will last a total of one hour for the volunteer (equipment, recording, de-equipping), including 30 minutes of acquisition.
Time frame: 1 hour
acquisition of ECG signals
Time frame: 1 hour
acquisition of peripheral and central photoplethysmographic signals with radial, brachial, carotid and femoral sensors
Time frame: 1 hour
acquisition of abdominal and thoracic section variations with an inductive plethysmographic vest
Time frame: 1 hour
Assesment of the link between peripheral and central vascular function with statistical analysis (Linear regression, Bland and Altman test)
Contact information is provided by the study sponsor or research team.
University Hospital, Grenoble
Other
Acronym: EvolVOAge
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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