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

  • STATUS
    Recruiting
  • End date
    Sep 30, 2025
  • participants needed
    120
  • sponsor
    Withings
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Updated on 6 May 2025
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Accepts healthy volunteers

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

Details
Condition Hypertension
Age 18years or above
Clinical Study IdentifierNCT06957847
SponsorWithings
Last Modified on6 May 2025

Eligibility

 Yes No Not Sure

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 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
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How to participate?

Step 1 Connect with a study center
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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