Hypertension - Atrial Fibrillation Clinical Trial
— DIMOSPAFOfficial title:
Association Between Circadian Blood Pressure Patterns With Asymptomatic Episodes of Paroxysmal Atrial Fibrillation in Hypertensive Subjects
Verified date | September 2015 |
Source | Evangelismos Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Greece: Ethics Committee |
Study type | Observational [Patient Registry] |
The goals of our study are to determine a).the association between abnormal circadian BP and the development of paroxysmal AF in hypertensive patients, b).at which level of TOD, paroxysmal AF episodes are detected in hypertensive subjects, c).if there is any association between systolic and/or diastolic BP levels with AF occurrence, d).whether the mean heart rate during a 24-hr interval is associated with the development of paroxysmal AF, and finally e).examine the relationship between a wide PP and asymptomatic AF episodes in patients with HTN.
Status | Not yet recruiting |
Enrollment | 200 |
Est. completion date | September 2016 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Patients diagnosed with essential HTN (office BP>140/90mmHg) or patients receiving at least one antihypertensive medication (ie. RAAA inhibitors or diuretic), aged 18-85 years of age. - Patients with at least one of the following risk factors, organ damage or other evidence of cardiovascular disease: - Previous stroke - Transient ischemic attack (TIA) - Systemic embolism - Diabetes mellitus type 2 - Obesity - Obstructive sleep apnea (OSA) - Dyslipidemia - History of coronary artery disease (CAD) - Valvular heart disease (VHD) - Echocardiographic findings attributed to HTN (ie. diastolic dysfunction, LVH) - White coat hypertension (WCH), masked hypertension (MH) - Positive family history for rhythm disturbances Exclusion Criteria: - Patients already diagnosed with paroxysmal or permanent AF - Severe renal insufficiency (eGFR according to MDRD formula <25ml/min/1.73m2) - Patients unable to attend follow-up visits - Clinical evidence of severe heart failure - Suspected secondary HTN - Mental disorders - Patients with cancer |
Observational Model: Cohort, Time Perspective: Cross-Sectional
Country | Name | City | State |
---|---|---|---|
Greece | Evangelismos General Hospital | Athens | Attiki |
Lead Sponsor | Collaborator |
---|---|
Evangelismos Hospital |
Greece,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Association between nighttime BP patterns and/or early morning surge with the development of asymptomatic episodes of paroxysmal atrial fibrillation in hypertensive subjects | • To investigate whether nighttime BP patterns (extreme dipping, normal dipping or reduced dipping and non-dipping including risers) or early morning surge are associated with the detection of paroxysmal AF in hypertensive subjects. | 12 months | No |
Secondary | Association between the degree of TOD and the development of paroxysmal AF in hypertensive patients | • To observe at which level of TOD, asymptomatic AF episodes are more commonly detected. | 12 months | No |
Secondary | Association between SBP and/or DBP levels with the development of paroxysmal AF in hypertensive patients | • To study if there is any relationship between systolic and/or diastolic BP levels with AF occurrence. | 12 months | No |
Secondary | Association between office heart rate or mean 24-hr heart rate with the development of asymptomatic paroxysmal AF episodes. | • To examine whether office HR or mean HR using ABPM is associated with the development of silent AF episodes. | 12 months | No |
Secondary | Association between PP and the development of asymptomatic paroxysmal AF episodes | • To examine whether a wide PP in ABPM is associated with the development of silent AF episodes. | 12 months | No |