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

NCT02823873 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2016-07-22

No results posted yet for this study

Summary

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.

Conditions

Interventions

DEVICE

Pulsewave oscillometric wrist cuff blood pressure monitor

Blood pressure monitor utilizing wrist cuff administered and measured using mobile technology.

Sponsors & Collaborators

  • University of Arkansas

    lead OTHER

Principal Investigators

  • Jill Mhyre, MD · University of Arkansas

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-07-31
Primary Completion
2017-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02823873 on ClinicalTrials.gov