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Clinical Trials/ACTRN12610000221055
ACTRN12610000221055
Completed
未知

Patients with atrial fibrillation undergoing a disease-specific patient management intervention programme compared to standard care for the optimisation of health and well-being

Baker IDI Heart & Diabetes Institute0 sites335 target enrollmentMarch 17, 2010
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Baker IDI Heart & Diabetes Institute
Enrollment
335
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 17, 2010
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Baker IDI Heart & Diabetes Institute

Eligibility Criteria

Inclusion Criteria

  • •1\. Documented diagnosis of sustained form of non\-valvular atrial fibrillation
  • •2\. A minimum of one hospitalisation (including index admission) related, at least in part, to atrial fibrillation
  • •3\. Are living independently in the community or their own home post\-hospitalisation
  • •4\. Are able and willing to provide written informed consent to participate in the trial

Exclusion Criteria

  • •1\. Aged below 45 years
  • •2\. Have a diagnosis of valvular atrial fibrillation
  • •3\. Are scheduled for a catheter ablation for treatment of atrial fibrillation
  • •4\. Have evidence of pre\-existing New York Heart Association (NYHA) Class III\-IV with a documented left ventricular ejection fraction less than 45%
  • •5\. Have alcohol\-induced atrial fibrillation
  • •6\. Have transient forms of atrial fibrillation associated with acute myocardial infarction and/or pericarditis
  • •7\. Have a terminal condition or malignancy requiring palliative care
  • •8\. Cannot adequately provide written informed consent to participate
  • •9\. Have any other medical condition that results in the belief that it is not appropriate for the patient to embark on participation within this study

Outcomes

Primary Outcomes

Not specified

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