NCT06957847

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

Clinical Validation Of The Brachial Blood Pressure Measuring Device Withings BPM Pro 2 According To "The Universal Protocol For The Validation Of Blood Pressure Measuring Devices By The Association For The Advancement Of Medical Instrumentation / European Society Of Hypertension / International Organization For Standardization (AAMI/ESH/ISO) (And Its Amendment 1 (2020) And 2 (2024))" In The General Population.

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 89 (actual)
• Sponsor: Withings · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

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

Conditions

• Hypertension

Interventions

Type	Name	Description
DEVICE	Blood pressure measurement	The patient will be measured alternatively with a reference mercury sphygmomanometer (four times) and the device under study (3 times)

Timeline

• Start date: 2025-04-28
• Primary completion: 2025-08-21
• Completion: 2025-11-18
• First posted: 2025-05-05
• Last updated: 2026-02-18

Locations

1 site across 1 country: Armenia