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
Recruiting
N/A
Interventional Study
Blood Pressure Measurement in Pregnancy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 40
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 500 (estimated)
- Sponsor
- Hillel Yaffe Medical Center · Government
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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
Trial Locations
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Eligibility Criteria
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)
Contacts