- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01132001
Ambulatory Versus Home Blood Pressure Measurement
October 9, 2012 updated by: George S. Stergiou, University of Athens
EVALUATION OF BLOOD PRESSURE MEASUREMENTS OUTSIDE OFFICE: COMPARISON OF DIAGNOSIS BASED ON EITHER AMBULATORY OR HOME BLOOD PRESSURE MEASUREMENTS
This is a prospective study comparing the three blood pressure monitoring methods on the diagnosis of arterial hypertension.
Blood pressure of each subject will be evaluated with clinic, home and 24h ambulatory blood pressure measurements in three visits
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Athens, Greece
- Recruiting
- Hypertension Center, Third Department of Medicine, University of Athens, Greece
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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
20 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Subjects referred to an outpatient hyperetension clinic for arterial hypertension
Description
Inclusion Criteria:
- Age > 20 yrs
- Patients referred to an outpatient clinic for high blood pressure
- Patients with no treatment or with antihypertensive treatment stable for at least 4 weeks.
- Patients capable of performing home blood pressure measurements.
- Signed informed consent
Exclusion Criteria:
- Hypertension stage III (SBP>180 mmHg or DBP>110mmHg)
- Secondary hypertension
- Resistant hypertension
- Arrhythmia
- Pregnancy
- Symptomatic heart disease
- Renal disease (Cr>2mg/dl)
- Uncontrolled diabetes mellitus (HbA1c>8.5%)
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood pressure monitoring methods
Time Frame: Baseline
|
Comparison among clinic, home and ambulatory blood pressure measurements.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: George S Stergiou, MD, Hypertension Center,Third Department of Medicine,University of Athens,Greece
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
October 1, 2009
Primary Completion (Anticipated)
November 1, 2012
Study Completion (Anticipated)
December 1, 2012
Study Registration Dates
First Submitted
May 26, 2010
First Submitted That Met QC Criteria
May 26, 2010
First Posted (Estimate)
May 27, 2010
Study Record Updates
Last Update Posted (Estimate)
October 11, 2012
Last Update Submitted That Met QC Criteria
October 9, 2012
Last Verified
October 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HBP5
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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