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Reduction of Atrial Fibrillation Study in Patients Undergoing Coronary Artery Bypass Grafting. (RASCABG 1 Study)

Primary Purpose

Atrial Fibrillation, Coronary Artery Bypass Grafting

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Amiodarone
Sponsored by
University of Aarhus
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atrial Fibrillation focused on measuring RASCABG 1 - study, Postoperative atrial fibrillation, Randomized, controlled trial, Amiodarone

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: enlistment for an elective CABG age more than 18 years willingness to be randomised provision of informed consent Exclusion Criteria: enlistment for other types of heart surgery earlier heart surgery resting heart rate below 40 bpm. AV-blockage of any degree preoperative atrial fibrillation or flutter former known atrial fibrillation or flutter lasting more than one month hepatic dysfunction (ALAT > twice the upper normal limit) hyperthyroidism pregnancy breastfeeding known adverse reactions to amiodarone

Sites / Locations

  • Department of Cardiothoracic and Vascular Surgery & Institute of Clinical Medicine, Skejby Sygehus, Aarhus University Hospital

Outcomes

Primary Outcome Measures

- Time to symptomatic atrial fibrillation, cerebral apoplexy/ transitory cerebral infarction (TCI), acute myocardial infarction (AMI), or death.
- Time to symptomatic or asymptomatic atrial fibrillation, cerebral apoplexy/TCI, AMI or death;
- Time to symptomatic or asymptomatic atrial fibrillation
- Time to symptomatic atrial fibrillation
All measured at postoperative day 7 and 30.

Secondary Outcome Measures

- Length of stay at Skejby Sygehus.
- Length of stay at Skejby Sygehus and local hospital.
- Length of stay at the intensive care unit (ICU) and intermediary unit, Skejby Sygehus

Full Information

First Posted
February 3, 2006
Last Updated
February 3, 2006
Sponsor
University of Aarhus
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1. Study Identification

Unique Protocol Identification Number
NCT00287209
Brief Title
Reduction of Atrial Fibrillation Study in Patients Undergoing Coronary Artery Bypass Grafting. (RASCABG 1 Study)
Official Title
Reduction of Atrial Fibrillation Study in Patients Undergoing Coronary Artery Bypass Grafting. (RASCABG 1 Study)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2006
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Aarhus

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine whether postoperatively oral treatment with high dosis amiodarone for five days after intravenously admitted bolusinfusion will minimize the risk for development of atrial fibrillation after coronary artery bypass grafting.
Detailed Description
New-onset atrial fibrillation (AF) after coronary bypass grafting (CABG) is common, with an incidence ranging from 5%-65%. Although postoperative atrial tachyarrhythmia is often regarded as a temporary problem related to the operation and therefore innocuous, this complication has clinically significant adverse effects on patient outcome. The purpose of this study was to find a good treatment without severe adverse effects to minimize the incidence of AF and maybe reduced the hemodynamic stress which AF is well known to cause. This would indicate that the risk of developing fatal events like cerebral apoplexy, TCI, AMI and death will be minimized as a result of the improved hemodynamic. Overall AF is associated with risk of illness and for the development of severe complications as cerebral apoplexy, TCI, AMI and death with a factor 2-3. There has furthermore been seen a twofold increase in the duration of intensive care unit stay and prolongation of the total hospitalization time with attendant increased hospitalization cost. The outbreak of AF after CABG has been increasing over the last twenty years. It is speculated that the reason for this rise in incidence is due to the advancing age in the patient populations, more complex cardiac surgery as due to former underestimation of the arrhythmia. Medical therapy includes various drugs, such as β-blockers, calcium channel blockers, digoxin, sotalol, quinidine, and amiodarone among others, to control heart rate and restore sinus rhythm. Most of these antiarrhythmic agents have significant cardiac and noncardiac adverse effects , why the use of these drugs should be minimized to a short period of time. Amiodarone is well known drug to treat AF and diminish the incidence of AF after CABG operation. So far there has not been any study focusing on postoperative high doses treatment with oral administrated amiodarone. The studies which have been publicized are studies where the drug was administrated intravenously pre-, post- or both pre- and postoperative. Some studies have orally administrated the drug in different regimes11 but no study has yet shown the possible affect of solitarily postoperative administrated high doses amiodarone after an intravenously administrated bolus, with the affect of getting loaded immediately.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Coronary Artery Bypass Grafting
Keywords
RASCABG 1 - study, Postoperative atrial fibrillation, Randomized, controlled trial, Amiodarone

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
250 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Amiodarone
Primary Outcome Measure Information:
Title
- Time to symptomatic atrial fibrillation, cerebral apoplexy/ transitory cerebral infarction (TCI), acute myocardial infarction (AMI), or death.
Title
- Time to symptomatic or asymptomatic atrial fibrillation, cerebral apoplexy/TCI, AMI or death;
Title
- Time to symptomatic or asymptomatic atrial fibrillation
Title
- Time to symptomatic atrial fibrillation
Title
All measured at postoperative day 7 and 30.
Secondary Outcome Measure Information:
Title
- Length of stay at Skejby Sygehus.
Title
- Length of stay at Skejby Sygehus and local hospital.
Title
- Length of stay at the intensive care unit (ICU) and intermediary unit, Skejby Sygehus

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: enlistment for an elective CABG age more than 18 years willingness to be randomised provision of informed consent Exclusion Criteria: enlistment for other types of heart surgery earlier heart surgery resting heart rate below 40 bpm. AV-blockage of any degree preoperative atrial fibrillation or flutter former known atrial fibrillation or flutter lasting more than one month hepatic dysfunction (ALAT > twice the upper normal limit) hyperthyroidism pregnancy breastfeeding known adverse reactions to amiodarone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vibeke E Hjortdal, Professor
Organizational Affiliation
Department of Cardiothoracic and Vascular Surgery & Institute of Clinical Medicine, Skejby Sygehus, Aarhus University Hospital, DK-8200 Aarhus N, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Cardiothoracic and Vascular Surgery & Institute of Clinical Medicine, Skejby Sygehus, Aarhus University Hospital
City
Aarhus N
ZIP/Postal Code
8200
Country
Denmark

12. IPD Sharing Statement

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Reduction of Atrial Fibrillation Study in Patients Undergoing Coronary Artery Bypass Grafting. (RASCABG 1 Study)

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