Actively Recruiting
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
Led by Hillel Yaffe Medical Center · Updated on 2026-01-06
500
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
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
Eligibility Criteria
You may qualify if you...
- Women aged 18-40
- Informed consent to participate
You will not qualify if you...
- Inability to cooperate with blood pressure measurement under optimal conditions
- Women with complex underlying disease that may bias the data (e.g. significant vasculopathy)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hille Yaffe Medical Center
Hadera, Israel, Israel, 3881000
Actively Recruiting
Research Team
I
Ikhlas IM Ammash, M.D
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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