Clinical Test for Armed-used Blood Pressure Monitor With Preformed Cuff(Monitor When Being Inflated)

This study has been completed.
Sponsor:
Information provided by:
Andon Health Co., Ltd
ClinicalTrials.gov Identifier:
NCT01206959
First received: September 21, 2010
Last updated: NA
Last verified: September 2010
History: No changes posted
  Purpose

The purpose of this study is to monitor the blood pressure level of the patient using a blood pressure monitor which test the blood pressure level in inflating state . The cuff range in the study is 22cm-48cm


Condition
Blood Pressure

Study Type: Observational
Study Design: Time Perspective: Prospective

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

Enrollment: 88
Groups/Cohorts
monitor method

blood pressure monitor Cuff circumference:22cm-48cm

stethoscopy Cuff circumference: 22cm-48cm


  Eligibility

Ages Eligible for Study:   40 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

hospital population, including patient and accompanies.

Criteria

Inclusion Criteria:

  • cuff circumference:22cm-48cm

Exclusion Criteria:

  • None
  Contacts and Locations
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, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Liu Yi, Andon Health Co., LTD
ClinicalTrials.gov Identifier: NCT01206959     History of Changes
Other Study ID Numbers: AndonHealth 4
Study First Received: September 21, 2010
Last Updated: September 21, 2010
Health Authority: China: Food and Drug Administration

Keywords provided by Andon Health Co., Ltd:
BP

ClinicalTrials.gov processed this record on July 28, 2014