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Blood Pressure Monitor Clinical Test (Cuff Range: 13.5 Cm-22cm)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01594307
First Posted: May 9, 2012
Last Update Posted: May 9, 2012
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 (Responsible Party):
Andon Health Co., Ltd
  Purpose
The purpose of this study is to monitor the blood pressure level of the patient using a preformed cuff ranged 13.5 cm-22 cm.

Condition
Blood Pressure

Study Type: Observational
Study Design: Time Perspective: Prospective

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

Enrollment: 85
Study Start Date: February 2012
Study Completion Date: April 2012
Groups/Cohorts
blood pressure monitor
Cuff circumference:13.5cm-22cm
stethoscopy
Cuff circumference: 13.5cm-22cm

  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 28 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
resident of a community
Criteria

Inclusion Criteria:

  • cuff circumference: 13.5cm-22cm
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Andon Health Co., Ltd
ClinicalTrials.gov Identifier: NCT01594307     History of Changes
Other Study ID Numbers: AndonHealth7
First Submitted: May 7, 2012
First Posted: May 9, 2012
Last Update Posted: May 9, 2012
Last Verified: April 2012

Keywords provided by Andon Health Co., Ltd:
BP