Clinical Validation of the Blood Pressure Measuring Device Withings BPM Pro 2 in Pregnancy and Pre-Eclampsia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWithings
About this trial
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
Eligibility criteria
Qualifiers
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;
Disqualifiers
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;
Trial design
Treatments tested in this trial
- Blood pressure measurement
Treatment groups
45 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov