Validation of Pulsewave Blood Pressure Monitor in Hypertensive and Normotensive Pregnant and Postpartum Women

Withdrawn before enrolling

Conditions studied: Hypertension

In brief

The purpose of this study is to test the accuracy of the Pulsewave wrist blood pressure cuff in pregnant and postpartum women who have either normal blood pressure or high blood pressure.

Key facts

Study ID

NCT02823873

Run by

University of Arkansas

People needed

0

Starts

2016-07-01

Last updated by the study team

2016-07-22

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Pregnant or admitted to the postpartum unit
• Normotensive women - No diagnosis of hypertension
• Hypertensive women - Diagnosis of hypertensive disorder of pregnancy

You may not qualify if…

• Women in active labor
• Women < 18 years of age
• Non-english speakers

Where it is running

• University of Arkansas for Medical Sciences — Little Rock, Arkansas, United States

Full record on ClinicalTrials.gov

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