Photoplethysmographic Measurements of Pulse Wave Velocity (PWV) and Blood Pressure (BP)
Recruiting
N/AInterventional Study
Healthy Volunteers
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
27 (estimated)
Sponsor
University Hospital, Grenoble · Other
Who this trial is looking for
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Theoretically, there is a correlation between the PWV and the value of the BP, mediated by the distensibility of the segment of artery where the measurements take place. The hypothesis is therefore that the measurement of the PWV through a multisite medical device for detecting the pulse wave by photoplethysmography makes it possible to deduce the value of the BP.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Healthy healthy volunteer subject,
* Aged 18 or over,
* Having expressed their consent to the research,
* Affiliated to a social security scheme,
* Registered in the national file of people who lend themselves to biomedical research
Exclusion Criteria:
* People referred to i…
Inclusion Criteria:
* Healthy healthy volunteer subject,
* Aged 18 or over,
* Having expressed their consent to the research,
* Affiliated to a social security scheme,
* Registered in the national file of people who lend themselves to biomedical research
Exclusion Criteria:
* People referred to in Articles L1121-5 to L1121-8 of the Public Health Code (corresponds to all protected persons: pregnant, parturient or breastfeeding women, persons deprived of liberty by judicial or administrative decision, persons subject of psychiatric care, minor, and person subject to a legal protection measure: guardianship, curatorship or safeguard of justice)
* Any history or presence of chronic illness
* Presence of Wolf Parkinson White ECG changes
* Subject with orthostatic hypotension
* People with an active implant (e.g. pacemaker)
* Known allergy or intolerance to silicone
* Orthostatic hypotension
* Cutaneous excoriations preventing the placement of sensors on the arms
* Patient with an active implant
* Subject cannot be contacted in case of emergency
* Taking treatment that may impact the recorded physiological measurements
* Subject in period of exclusion from another clinical investigation
* Subject who would receive more than 4500 euros in compensation due to his participation in other biomedical research in the 12 months preceding this study
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