Checking the accuracy of the Withings BPM Pro 2 blood pressure monitor in pregnancy
Tests how accurately an upper-arm blood pressure monitor measures in pregnant women, including pre-eclampsia.
Plain-language title generated from the registry record
Registry title: Clinical Validation of the Blood Pressure Measuring Device Withings BPM Pro 2 in Pregnancy and Pre-Eclampsia
Key facts
- Where
- Yerevan, ArmeniaSee the site
Where in Armenia
- N2Yerevan, ArmeniaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Withings
- Trial code
- NCT07595016
- Record updated
- 3 June 2026
- Original description
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-eclampsiaRead full original descriptionShow less
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 Pregnancy And Pre-Eclampsia
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
Inclusion: 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.
Exclusion: Patient suffering from arrhythmia; Patient unable to give a consent or understand properly protocol information; 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.