Atrial Fibrillation Clinical Trial
Official title:
A Comparison of the Effectiveness of Carvedilol Versus Metoprolol for Atrial Fibrillation Appearing After Off-Pump Coronary Bypass Surgery in the Carvedilol or Metoprolol Post-Revascularization Atrial Fibrillation Controlled Trial (COMPACT)
| NCT number | NCT00198614 |
| Other study ID # | 16C-9 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | September 13, 2005 |
| Last updated | February 28, 2007 |
| Start date | January 2005 |
Postoperative new-onset atrial fibrillation (AF) is the most common complication stemming from coronary artery bypass graft surgery, and is associated with increased early and late mortality risk. Standard guidelines recommend β blockers for the prevention of AF; however, no prospective study has compared the relative efficacy of β-blocking agents. We hypothesize that carvedilol, a non-selective adrenergic blocker with both anti-inflammatory and antioxidant properties, is more effective than metoprolol, a conventional β1-selective antagonist, in suppressing new-onset AF following off-pump coronary bypass surgery. We have designed the Carvedilol or Metoprolol Post-Revascularization Atrial Fibrillation Controlled Trial (COMPACT) to test our hypothesis in a multi-center, open-label, and randomized controlled trial.
| Status | Completed |
| Enrollment | 650 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 20 Years to 89 Years |
| Eligibility |
Inclusion criteria: Adult male or female patients are required to meet the following criteria: 1. Aged 20 to 89 years 2. Underwent isolated off-pump coronary artery bypass graft surgery 3. Written informed consent Exclusion criteria: Patients with the following conditions will be excluded from the study: 1. Pre- and intraoperative use of mechanical circulatory support devices, except an intra-aortic balloon pump 2. Concomitant operations, such as aneurysmectomy or carotid endarterectomy 3. Surgical approaches other than a median full sternotomy 4. Acute myocardial infarction ?3 days before enrollment in the trial 5. Contraindication against treatment with ß blockers 6. Presence of preoperative chronic AF or flutter 7. History of paroxysmal AF 8. Presence of antidysrhythmic medication other than ß blockers, calcium channel blockers, or digitalis 9. A resting heart rate of less than 50 beats/min in the absence of medical therapy known to slow the sinus rate 10. Endocrine disorders, such as pheochromocytoma, active hyperthyroidism, and untreated hypothyroidism 11. Pregnant women and females with childbearing potential unless utilizing adequate contraception 12. Preoperative need for a temporary or permanent pacemaker 13. Non-interpretable electrocardiogram for P wave assessment 14. Undergoing treatment for asthma or other chronic obstructive pulmonary disease 15. Second- or third-degree atrioventricular block 16. Sick sinus syndrome 17. Uncontrolled heart failure 18. Unstable insulin-dependent diabetes mellitus 19. Steroid therapy requirement 20. History of autoimmune diseases 21. Active infectious diseases, including myocarditis or pericarditis 22. Any other serious disease that could potentially complicate the management and follow-up protocols |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
| Country | Name | City | State |
|---|---|---|---|
| Japan | National Cardiovascular Center | Suita | Osaka |
| Lead Sponsor | Collaborator |
|---|---|
| Ministry of Health, Labour and Welfare, Japan |
Japan,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The primary endpoint is the incidence of new-onset AF during the first seven days after surgery; AF is defined as an episode of atrial fibrillation or flutter lasting for >30 seconds as detected on the continuous cardiac monitor. | |||
| Secondary | the incidence, duration, and recurrence of new-onset AF after surgery and before hospital discharge | |||
| Secondary | the frequency of external or internal electrical cardioversion after surgery and before hospital discharge | |||
| Secondary | the incidence of AF rhythm at hospital discharge | |||
| Secondary | premature discontinuation of assigned drug administration | |||
| Secondary | in-hospital mortality for any cause after surgery | |||
| Secondary | in-hospital morbidity after surgery | |||
| Secondary | resource use after surgery until hospital discharge. |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05654272 -
Development of CIRC Technologies
|
||
| Completed |
NCT04571385 -
A Study Evaluating the Efficacy and Safety of AP30663 for Cardioversion in Participants With Atrial Fibrillation (AF)
|
Phase 2 | |
| Terminated |
NCT04115735 -
His Bundle Recording From Subclavian Vein
|
||
| Completed |
NCT05366803 -
Women's Health Initiative Silent Atrial Fibrillation Recording Study
|
N/A | |
| Completed |
NCT02864758 -
Benefit-Risk Of Arterial THrombotic prEvention With Rivaroxaban for Atrial Fibrillation in France
|
||
| Recruiting |
NCT05442203 -
Electrocardiogram-based Artificial Intelligence-assisted Detection of Heart Disease
|
N/A | |
| Completed |
NCT05599308 -
Evaluation of Blood Pressure Monitor With AFib Screening Feature
|
N/A | |
| Completed |
NCT03790917 -
Assessment of Adherence to New Oral anTicoagulants in Atrial Fibrillation patiEnts Within the Outpatient registrY
|
||
| Enrolling by invitation |
NCT05890274 -
Atrial Fibrillation (AF) and Electrocardiogram (EKG) Interpretation Project ECHO
|
N/A | |
| Recruiting |
NCT05266144 -
Atrial Fibrillation Patients Treated With Catheter Ablation
|
||
| Recruiting |
NCT05316870 -
Construction and Effect Evaluation of Anticoagulation Management Model in Atrial Fibrillation
|
N/A | |
| Not yet recruiting |
NCT06023784 -
The Impact of LBBAP vs RVP on the Incidence of New-onset Atrial Fibrillation in Patients With Atrioventricular Block
|
N/A | |
| Recruiting |
NCT05572814 -
Transform: Teaching, Technology, and Teams
|
N/A | |
| Recruiting |
NCT04092985 -
Smart Watch iECG for the Detection of Cardiac Arrhythmias
|
||
| Completed |
NCT04087122 -
Evaluate the Efficiency Impact of Conducting Active Temperature Management During Cardiac Cryoablation Procedures
|
N/A | |
| Completed |
NCT06283654 -
Relieving the Emergency Department by Using a 1-lead ECG Device for Atrial Fibrillation Patients After Pulmonary Vein Isolation
|
||
| Recruiting |
NCT05416086 -
iCLAS™ Cryoablation System Post-Market Clinical Follow-up (PMCF) Study
|
N/A | |
| Completed |
NCT05067114 -
Solutions for Atrial Fibrillation Edvocacy (SAFE)
|
||
| Completed |
NCT04546763 -
Study Watch AF Detection At Home
|
||
| Completed |
NCT03761394 -
Pulsewatch: Smartwatch Monitoring for Atrial Fibrillation After Stroke
|
N/A |