Clinical Test for Armed-used Blood Pressure Monitor With Preformed Cuff

This study has been completed.
Sponsor:
Information provided by:
Andon Health Co., Ltd
ClinicalTrials.gov Identifier:
NCT01001455
First received: October 23, 2009
Last updated: NA
Last verified: October 2009
History: No changes posted
  Purpose

The purpose of this study is to monitor the blood pressure level of the patient using a preformed cuff ranged 22 cm-36 cm.


Condition
Blood Pressure

Study Type: Observational
Study Design: Time Perspective: Prospective

Further study details as provided by Andon Health Co., Ltd:

Primary Outcome Measures:
  • level of blood pressure [ Time Frame: 10S ] [ Designated as safety issue: No ]

Enrollment: 90
Study Start Date: August 2009
Study Completion Date: October 2009
Primary Completion Date: October 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
blood pressure monitor
Cuff circumference:22cm-36cm
stethoscopy
Cuff circumference: 22cm-36cm

  Eligibility

Ages Eligible for Study:   23 Years to 84 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

resident of a community.

Criteria

Inclusion Criteria:

  • cuff circumference:22cm-36cm

Exclusion Criteria:

  • None
  Contacts and Locations
No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Liu Yi, Andon Health co., LTD
ClinicalTrials.gov Identifier: NCT01001455     History of Changes
Other Study ID Numbers: AndonHealth3
Study First Received: October 23, 2009
Last Updated: October 23, 2009
Health Authority: China: Food and Drug Administration

Keywords provided by Andon Health Co., Ltd:
BP

ClinicalTrials.gov processed this record on April 14, 2014