A Clinical Evaluation of Omron Digital Blood Pressure Monitor
NCT ID: NCT03130686
Last Updated: 2017-04-26
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
92 participants
OBSERVATIONAL
2015-12-21
2016-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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OMRON blood pressure monitor HEM-9210T
To measure systolic blood pressure, diastolic blood pressure and pulse rate in patients.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* When body motion is observed during measurement.
* Korotkoff sound is poor quality.
* Patient's arm circumference is outside cuff range.
* Patient's auscultatory systolic blood pressure readings differ by more than 12mmHg. and patient's diastolic blood pressure readings differ by more than 8mmHg.
* Patients stated they did not wish to continue with the study and it is stopped before completion.
18 Years
ALL
Yes
Sponsors
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Biwako Chuo Hospital Japan
UNKNOWN
Shared Care Research and Education Consulting,. Inc. US
UNKNOWN
Omron Healthcare Co., Ltd.
INDUSTRY
Responsible Party
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Locations
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OMRON HEALTHCARE CO., Ltd.
Mukō, , Japan
Countries
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Other Identifiers
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HDV-TCD-150311
Identifier Type: -
Identifier Source: org_study_id
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