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OpenTrials
Completed

NCT Number: NCT02021994

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

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

Completed

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Key information

Conditions

Age range

20 year–83 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Normal adult or adults with Hypertension

Exclusion criteria

⎯1) people with serious arrhythmia

  • Patients with Takayasu arteritis
  • people wit adverse vascular peripheral circulation
  • people with upper limbs vein thrombosis
  • people who is weak

Treatment and study plan

Primary outcomes

  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

Sponsors and collaborators

Lead sponsor

Andon Health Co., Ltd

Industry

Registry information

Important dates

Study start
2013
Primary completion
2013
First posted
Dec 27, 2013
Registry last updated
Dec 27, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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