Can this smart blood pressure cuff get it right?
NCT ID NCT06957847
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study checked how well the Withings BPM Pro 2, an automatic blood pressure cuff, measures blood pressure compared to a standard manual device. 89 adults had their blood pressure taken with both devices. The goal was to see if the Withings cuff is accurate enough for home use. The study is already finished.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Withings BPM Pro 2 blood pressure monitor
- What this could lead to
- If successful, this could confirm that the Withings BPM Pro 2 is a reliable home blood pressure monitor for general use.
- What could go wrong
- This is a small, completed validation study, not a treatment trial. It only checks accuracy, not health outcomes. Results may not apply to people with arrhythmia or very large/small arms.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
89 people
The number who actually took part.
- Started
-
Apr 2025
- Finished
-
Nov 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
N2
Yerevan, 0002, Armenia
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Other studies related to the condition(s) this trial covers.
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