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Blood Pressure Monitor Clinical Test (Cuff Range: 22 Cm-42cm)

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.
 
ClinicalTrials.gov Identifier: NCT01575067
Recruitment Status : Completed
First Posted : April 11, 2012
Last Update Posted : April 11, 2012
Sponsor:
Information provided by (Responsible Party):
Andon Health Co., Ltd

Tracking Information
First Submitted Date April 9, 2012
First Posted Date April 11, 2012
Last Update Posted Date April 11, 2012
Study Start Date February 2012
Actual Primary Completion Date April 2012   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History No Changes Posted
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Blood Pressure Monitor Clinical Test (Cuff Range: 22 Cm-42cm)
Official Title Not Provided
Brief Summary The purpose of this study is to monitor the blood pressure level of the patient using a preformed cuff ranged 22 cm-42 cm.
Detailed Description Not Provided
Study Type Observational
Study Design Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population resident of a community
Condition Blood Pressure
Intervention Not Provided
Study Groups/Cohorts
  • blood pressure monitor
    Cuff circumference:22cm-42cm
  • stethoscopy
    Cuff circumference: 22cm-42cm
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: April¬†10,¬†2012)
85
Original Actual Enrollment Same as current
Actual Study Completion Date April 2012
Actual Primary Completion Date April 2012   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • cuff circumference: 22cm-42cm
Sex/Gender
Sexes Eligible for Study: All
Ages 30 Years to 84 Years   (Adult, Older Adult)
Accepts Healthy Volunteers Yes
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Not Provided
Removed Location Countries  
 
Administrative Information
NCT Number NCT01575067
Other Study ID Numbers AndonHealth5
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Andon Health Co., Ltd
Study Sponsor Andon Health Co., Ltd
Collaborators Not Provided
Investigators Not Provided
PRS Account Andon Health Co., Ltd
Verification Date April 2012