Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 October 2017 |
Main ID: |
NCT01120990 |
Date of registration:
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06/05/2010 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Hybrid Blood Pressure Monitor Validation
NISSEI |
Scientific title:
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Validation of a Hybrid Blood Pressure Monitor to Replace the Mercury Standard for Validation Studies According to Modified Criteria of the European Society of Hypertension International Protocol 2010 |
Date of first enrolment:
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April 2010 |
Target sample size:
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51 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT01120990 |
Study type:
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Interventional |
Study design:
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Phase:
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Phase 4
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Countries of recruitment
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Greece
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Contacts
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Name:
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George S Stergiou, MD |
Address:
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Telephone:
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Email:
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Affiliation:
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Hypertension Center, Third Depertment of Medicine, University of Athens, Greece |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Above 25 years of age
- Sinus rhythm
- Informed consent
Exclusion Criteria:
- Sustained arrhythmia
- Pregnancy
- Poor quality Korotkoff sounds
- Unavailable cuff size
- Completed blood pressure range (according to protocol)
Age minimum:
25 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Essential Hypertension
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Intervention(s)
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Other: Blood Pressure Measurement
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Primary Outcome(s)
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Diastolic Blood Pressure Measured With Mercury Sphygmomanometer.
[Time Frame: 3 months]
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Systolic Blood Pressure Measured by Tested Device.
[Time Frame: 3 months]
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Systolic Blood Pressure Measured With Mercury Sphygmomanometer.
[Time Frame: 3 months]
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Diastolic Blood Pressure Measured by Tested Device.
[Time Frame: 3 months]
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Secondary ID(s)
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Hybrid BP Monitor Validation
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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