Use of Fish Oils to Reduce Recurrence of Atrial Fibrillation Following DC Cardioversion

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2005 by Melbourne Health.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Melbourne Health
ClinicalTrials.gov Identifier:
NCT00232219
First received: October 2, 2005
Last updated: NA
Last verified: October 2005
History: No changes posted

October 2, 2005
October 2, 2005
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No Changes Posted
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Use of Fish Oils to Reduce Recurrence of Atrial Fibrillation Following DC Cardioversion
Use of Fish Oils to Reduce Recurrence of Atrial Fibrillation Following DC Cardioversion.

The purpose of this study is to investigate whether fish oil supplements may be beneficial in preventing the recurrence of atrial fibrillation after cardioversion.

Atrial fibrillation is a heart condition which can sometimes be successfully treated by a cardioversion.

Cardioversion involves resetting the heart back to normal with the use of electric current.

There is a tendency for the atrial fibrillation to recur , days weeks or even months after the cardioversion.

Fish oil supplements may be of benefit to patients with heart problems Recent evidence suggests that fish oils may be beneficial to patients with rhythm disturbances.

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Interventional
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Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Atrial Fibrillation
Drug: Fish oil
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
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Inclusion Criteria:

  • Patients with persistent Atrial Fibrillation on Warfarin.

Exclusion Criteria:

  • paroxysmal atrial fibrillation with self terminating episodes.
  • left atrial size>6.0cm
  • myocardial infarction in the previous 6 months.
  • contraindications to amiodarone use .
  • cardiac surgery in the previous 3 months .
  • an acute reversible illness contributing to the development of af
  • a QTc interval > 480ms.
  • pregnancy
Both
18 Years to 80 Years
Yes
Contact: Paul Sparks, MBBS,PhD, FRACP 0393427000 ext 27133 paul.sparks@mh.org.au
Australia
 
NCT00232219
2003.188
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Melbourne Health
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Principal Investigator: Paul Sparks, MBBS, PhD. FRACP Melbourne Health
Melbourne Health
October 2005

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