RecruitingNot Applicable

The Aim of the Study is to Examine the Variation in Blood Pressure Between an Optimal Measurement (According to Established Guidelines in the Literature - Per Guidelines) and a 'Common' Measurement (Used by Nursing Teams - Per Common Practice) Among Women of Reproductive Age With and Without Hyperte

Israel500 participantsStarted 2025-08-24

Plain-language summary

The aim of the study is to examine the variation in blood pressure between an optimal measurement (according to established guidelines in the literature - per guidelines) and a 'common' measurement (used by nursing teams - per common practice) among women of reproductive age with and without hyperte

Who can participate

Age range18 Years – 40 Years

SexFEMALE

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Inclusion Criteria: * Women aged 18-40 * Informed consent to participate. Exclusion Criteria: * Inability to cooperate with BP measurement under optimal conditions * Women with complex underlying disease that may bias the data (e.g. significant vasculopathy)

What they're measuring

Mean difference in systolic blood pressure (mmHg) between guideline-based and routine clinical measurement

Timeframe: 1 year

Trial details

NCT IDNCT07320339

SponsorHillel Yaffe Medical Center

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2026-08-24

Contact for this trial

Ikhlas IM Ammash, M.D

+972-4-7744602 AnnaTu@hymc.gov.il

View on ClinicalTrials.gov More Blood Pressure Measurement in Pregnancy trials