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Wrist-used Blood Pressure Monitor Clinical Test (Cuff Range: 14cm-25cm) (WBPMCT)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00952965
First Posted: August 6, 2009
Last Update Posted: August 7, 2009
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.
Information provided by:
Andon Health Co., Ltd
  Purpose
The purpose of this study is to monitor the blood pressure level of the patient using a wrist cuff ranged 14 cm-25 cm.

Condition
Blood Pressure

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Clinical Testing Report for Wrist-used Electronic Blood Pressure Monitor

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

Primary Outcome Measures:
  • level of blood pressure [ Time Frame: 10 s ]

Enrollment: 86
Study Start Date: April 2009
Study Completion Date: July 2009
Primary Completion Date: July 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
blood pressure monitor
wrist circumference: 14cm-25cm
stethoscopy
wrist circumference: 14cm-25cm

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   23 Years to 81 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
resident of a community.
Criteria

Inclusion Criteria:

  • wrist circumference: 14 cm-25 cm

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00952965


Locations
China, Tianjin
Beichen hospital
Tianjin, Tianjin, China, 300000
Sponsors and Collaborators
Andon Health Co., Ltd
Investigators
Principal Investigator: Qi Sun Andon Health Co., Ltd
  More Information

Publications:
Responsible Party: Liu Yi, Andon Health co., LTD
ClinicalTrials.gov Identifier: NCT00952965     History of Changes
Other Study ID Numbers: AndonHealth2
First Submitted: August 5, 2009
First Posted: August 6, 2009
Last Update Posted: August 7, 2009
Last Verified: August 2009

Keywords provided by Andon Health Co., Ltd:
BP