EICHORCondition: Hypertension · Pre-eclampsia · Sponsor: Withings
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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
This description comes directly from the study's public registry record.
Inès Bedouda · 0141460460 · clinical-trials@withings.com
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Inclusion Criteria: * 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 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.
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| N2 | Yerevan, Armenia, Armenia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07595016