Blood Pressure Assessment in Atrial Fibrillation

This study is currently recruiting participants. (see Contacts and Locations)
Verified September 2013 by University of Athens
Sponsor:
Information provided by (Responsible Party):
George S. Stergiou, University of Athens
ClinicalTrials.gov Identifier:
NCT01088269
First received: March 16, 2010
Last updated: September 20, 2013
Last verified: September 2013

March 16, 2010
September 20, 2013
March 2010
March 2014   (final data collection date for primary outcome measure)
Blood Pressure Measurement in Atrial Fibrillation,Serum Markers and echocardiographic indexes in atrial fibrillation (AF) [ Time Frame: Baseline ] [ Designated as safety issue: No ]
  1. Evaluation of the oscillometric technique of an electronic device in blood pressure measurement.
  2. Evaluation of the relationship of blood pressure levels with serum markers and ultrasonographic cardiac indexes.
Blood Pressure Measurement in Atrial Fibrillation,Serum Markers and echocardiographic indexes in AF [ Time Frame: Baseline ] [ Designated as safety issue: No ]
  1. Evaluation of the oscillometric technique of an electronic device in blood pressure measurement.
  2. Evaluation of the relationship of blood pressure levels with serum markers and ultrasonographic cardiac indexes.
Complete list of historical versions of study NCT01088269 on ClinicalTrials.gov Archive Site
Not Provided
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Blood Pressure Assessment in Atrial Fibrillation
Evaluation of the Oscillometric Blood Pressure Measurement in Atrial Fibrillation and Relation of Blood Pressure With Serum Biomarkers and Echocardiographic Indexes

This is a cross-sectional study including patients with permanent atrial fibrillation. Assessment will include:

  • clinic blood pressure measurements (mercury sphygmomanometer and automated oscillometric device)
  • 24-hour ambulatory blood pressure monitoring
  • determination of various serum markers and cardiac ultrasound.
Not Provided
Observational
Observational Model: Case Control
Time Perspective: Cross-Sectional
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Non-Probability Sample

SUBJECTS REFERRED TO HYPERTENSION CENTER

Atrial Fibrillation
Not Provided
  • AF
    Hypertensive patients in AF
  • Non-AF
    Hypertensive Patients
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
70
September 2014
March 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Hypertensives adults in atrial fibrillation

Exclusion Criteria:

  • Renal disease (Cr > 2 mg/l).
  • Patients with pacemaker rhythm during the study.
  • Each patient with acute disease (inflammation, surgery), malignancy, collagen diseases, pulmonary fibrosis, renal failure, liver failure, chronic inflammatory diseases.
Both
25 Years to 85 Years
No
Contact: George S Stergiou, MD +302107763117 gstergi@med.uoa.gr
Greece
 
NCT01088269
BPM IN AF
No
George S. Stergiou, University of Athens
University of Athens
Not Provided
Study Chair: George S Stergiou, MD Hypertension Center,Third Department of Medicine,University of Athens,Greece
University of Athens
September 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP