Blood Pressure Monitor Clinical Test (Cuff Range: 22 cm-30 cm)

May 18, 2009 updated by: Andon Health Co., Ltd
The purpose of this study is to monitor the blood pressure level of the patient using a cuff ranged 22 cm-30 cm.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

85

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

People whose arm range is 22 cm-30 cm

Description

Inclusion Criteria:

  • arm range: 22 cm-30 cm

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
stethoscopy
BPM
blood pressure monitor

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Andon Health Co., Ltd

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2009

Primary Completion (Actual)

April 1, 2009

Study Registration Dates

First Submitted

May 14, 2009

First Submitted That Met QC Criteria

May 18, 2009

First Posted (Estimate)

May 19, 2009

Study Record Updates

Last Update Posted (Estimate)

May 19, 2009

Last Update Submitted That Met QC Criteria

May 18, 2009

Last Verified

May 1, 2009

More Information

Terms related to this study

Other Study ID Numbers

  • AndonHealth1

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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