Clinical Validation of the Blood Pressure Measuring Device Withings BPM Pro 2 (WIHYP-GP)

Phase

N/A

Condition

Williams Syndrome

Vascular Diseases

Stress

Treatment

Blood pressure measurement

Clinical Study ID

NCT06957847

2025-A00050-49

Ages > 18
All Genders
Accepts Healthy Volunteers

Study Summary

The aim of the study is to assess the accuracy of the automatic oscillometric BP measuring device at the brachial level, the WITHINGS BPM Pro 2, in the general population

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patient older than 18 years;
Patient who signed the informed consent form;
Patient followed-up at site (in-patient or out-patient);
Patient with arm circumference between 22 cm and 42 cm.

Exclusion

Exclusion Criteria:

Patient unable to give a consent or understand properly protocol information;
Patient suffering from arrhythmia;
Patient with poor quality of Korotkov sounds;
Patient for whom K5 sounds are absent;
Patient wearing an implantable electric medical device (pacemaker,…);
Patient with both upper arms suffering from open wound and/or damaged skin.

Study Design