Emergency Department Home Blood Pressure Monitoring and BpTRU Study
NCT ID: NCT02217059
Last Updated: 2017-11-29
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
105 participants
OBSERVATIONAL
2014-08-31
2017-07-31
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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COHORT
PROSPECTIVE
Study Groups
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Prehypertension
Using the JNC7 definition
No interventions assigned to this group
Stage I Hypertension
Using the JNC7 definition
No interventions assigned to this group
Stage II Hypertension
Using the JNC7 definition
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* BpTRU device blood pressure greater than 120 systolic and/or 80 diastolic while in ED
Exclusion Criteria
* Currently on antihypertensives or receiving prescription on discharge
* Pregnancy
* History of atrial fibrillation
* Dialysis patient
* Nursing home or rehabilitation center resident
* Admitted
* Moving out of the area in next 30 days
* Substance abuse
* Prisoner
* Presenting for psychiatric complaint requiring constant observation
* Inability to give informed consent (intoxicated, altered, non-English speaking)
* Presenting with symptoms of hypertensive emergency
* Inability to demonstrate adequate use of the home blood pressure device in the ED
* Arm circumference less than 9 inches or greater than 17 inches
18 Years
ALL
Yes
Sponsors
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Rhode Island Hospital
OTHER
Responsible Party
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Locations
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Rhode Island Hospital
Providence, Rhode Island, United States
Countries
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Other Identifiers
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UEMF0000
Identifier Type: -
Identifier Source: org_study_id