Clinical Validation of the Blood Pressure Measuring Device Withings BPM Pro 2 in Pregnancy and Pre-Eclampsia

Recruiting now · Not applicable

Conditions studied: Hypertension, Pre-eclampsia

In brief

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 pregnancy and pre-eclampsia

Key facts

Study ID

NCT07595016

Run by

Withings

People needed

45

Starts

2026-05-11

Expected to finish

2026-09-30

Last updated by the study team

2026-06-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patient older than 18 years;
• Known pregnancy, in second or third trimester of pregnancy ( > 3 months);
• Patient normotensive, hypertensive or in preeclampsia;
• 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.

You may not qualify if…

• 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.

Where it is running

• N2 — Yerevan, Armenia, Armenia (enrolling)

Full record on ClinicalTrials.gov

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