Measuring Blood Pressure in Pregnancy Using Mercury and Automated Device
NCT ID: NCT00809666
Last Updated: 2008-12-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
220 participants
INTERVENTIONAL
2000-05-31
2006-09-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
SINGLE_GROUP
DIAGNOSTIC
SINGLE
Study Groups
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Mercury
All subsequent blood pressure recording done using mercury sphygmomanometry
Automated blood pressure recording device Omron HEM 705CP
All subsequent blood pressure recordings done using the automated device
Interventions
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Automated blood pressure recording device Omron HEM 705CP
All subsequent blood pressure recordings done using the automated device
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
16 Years
45 Years
FEMALE
Yes
Sponsors
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St George Hospital, Australia
OTHER
Responsible Party
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St George Hospital and UNSW
Locations
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St George Hospital
Sydney, New South Wales, Australia
Countries
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References
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High blood pressure research Council of Australia. Position Statement on the replacement of mercury sphygmomanometers. September 2006. www.hbprca.com.au
Ashworth DC, Maule SP, Stewart F, Nathan HL, Shennan AH, Chappell LC. Setting and techniques for monitoring blood pressure during pregnancy. Cochrane Database Syst Rev. 2020 Jul 23;8(8):CD012739. doi: 10.1002/14651858.CD012739.pub2.
Other Identifiers
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00/41 Brown
Identifier Type: -
Identifier Source: org_study_id