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

ConditionBlood Pressure Measurement in Pregnancy

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

Age18-40

SponsorHillel Yaffe Medical Center

About this trial

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

Eligibility criteria

Qualifiers

Women aged 18-40

Informed consent to participate.

Disqualifiers

Inability to cooperate with BP measurement under optimal conditions

Women with complex underlying disease that may bias the data (e.g. significant vasculopathy)

Trial design

Treatments tested in this trial

blood pressure measurement

Treatment groups

500 Participants

are divided into 1 treatment group

Sponsors and collaborators

Hillel Yaffe Medical Center

Lead sponsor

Source ClinicalTrials.gov