Comparisons of mercury-free and automated sphygmomanometers with mercury sphygmomanometry in hypertensive and normotensive pregnant women: parallel, prospective, observational study

Not Applicable

Completed

• Conditions: Blood pressure in pregnancy; Reproductive Health and Childbirth - Fetal medicine and complications of pregnancy

• Registration Number: ACTRN12613001262796
• Lead Sponsor: Prof Mark Brown

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2013-11-18
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 340

Inclusion Criteria

Hypertensive and normotensive pregnant women in their third trimester

Exclusion Criteria

None

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main outcome measures were the percentages of readings of test devices that were within 5, 10, and 15 mm Hg difference from the readings with mercury sphygmomanometry[At time of blood pressure measurement]

Secondary Outcome Measures

Name	Time	Method
il[Nil]