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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02021994
Recruitment Status : Completed
First Posted : December 27, 2013
Last Update Posted : December 27, 2013
Sponsor:
Information provided by (Responsible Party):
Andon Health Co., Ltd

Brief Summary:

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


Condition or disease
Blood Pressure

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Study Type : Observational
Actual Enrollment : 85 participants
Time Perspective: Prospective
Study Start Date : June 2013
Actual Primary Completion Date : September 2013

Group/Cohort
Arm Automatic Electronic BPM
mercury sphygmomanometer



Primary Outcome Measures :
  1. All the test results of the electronic blood pressure monitor with 5 cuffs is within the accuracy creteria, with the mercury sphygmomanometer as control [ Time Frame: 1 day ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 83 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
resident of a community
Criteria

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
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Responsible Party: Andon Health Co., Ltd
ClinicalTrials.gov Identifier: NCT02021994    
Other Study ID Numbers: Andon Health 9
First Posted: December 27, 2013    Key Record Dates
Last Update Posted: December 27, 2013
Last Verified: December 2013