BPM Cuff: 15-24cm, 20-34cm, 30-44cm, 40-48cm, 22-42cm

NCT ID: NCT02021994

Last Updated: 2013-12-27

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

85 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-06-30

Brief Summary

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The purpose of this study is to verify the accuracy of the 5 blood pressure cuffs, with blood pressure monitor device.

The cuff range is as follows:

15cm-24cm, 20cm-34cm, 30cm-44cm, 40cm-48cm, and 22cm-42cm

Detailed Description

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Conditions

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Blood Pressure

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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Arm Automatic Electronic BPM

No interventions assigned to this group

mercury sphygmomanometer

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Normal adult or adults with Hypertension

Exclusion Criteria

⎯1) people with serious arrhythmia
2. Patients with Takayasu arteritis
3. people wit adverse vascular peripheral circulation
4. people with upper limbs vein thrombosis
5. people who is weak
Minimum Eligible Age

20 Years

Maximum Eligible Age

83 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Andon Health Co., Ltd

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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Andon Health 9

Identifier Type: -

Identifier Source: org_study_id