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Clinical Trials/NCT00486915
NCT00486915
Completed
Not Applicable

Concurrent Prophylactic Left Atrial Appendage Exclusion: A Randomized Controlled Trial

London Health Sciences Centre1 site in 1 country43 target enrollmentApril 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
London Health Sciences Centre
Enrollment
43
Locations
1
Primary Endpoint
Incidence of Stroke
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Stroke is a major cause of morbidity in western society, and an infrequent complication of cardiac surgery. The majority of thromboembolic strokes arise from the left atrium, in particular the left atrial appendage. This study aims to assess the short-term effects of left atrial appendage ligation in terms of postoperative clinical and biochemical parameters; and the long-term effects of left atrial appendage ligation in terms of stroke incidence.

Detailed Description

In patients with non-rheumatic atrial fibrillation, the left atrial appendage is the origin of at least 90% of all left atrial clots, and the resulting systemic emboli cause approximately 25% of all strokes. The stroke rate in patients with atrial fibrillation older than 75 years of age is 8.1% per year with one clinical risk factor and is 12% per year at any age in clinical trial populations with a history of prior thromboembolism. Three-year stroke rates in elderly nursing home patients not anticoagulated are in excess of 50% (Atrial Fibrillation Investigators 1994). Anticoagulation is oftentimes withheld due to the perception of excessive risk in case of a fall; even when anticoagulation is prescribed, it is well known that therapeutic levels are not always maintained. Left atrial appendage obliteration is commonly performed in a variety of cardiac surgical operations. There have been animal studies and theoretical arguments which demonstrate the importance of the atrial appendage in its role to support cardiac output and blood pressure, and modulate thirst and hypercoagulability (Stollberger 2003); however this has been poorly studied and documented in humans in the available literature. BNP and ANP have been shown to increase proportionately with left atrial appendage dysfunction, as have von Willebrands Factor, D-Dimer, and thrombin-antithrombin III complex (Igarashi 2001). To date, there is not a single randomized controlled trial with adequate follow-up to assess the short- and long-term clinical effectiveness of concurrent prophylactic LAA ligation. This trial will fill that void.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
December 2012
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dave Nagpal

Associate Professor of Cardiac Surgery and Critical Care Medicine, Surgical Director of Heart Failure and Mechanical Circulatory Support Program

London Health Sciences Centre

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing mitral valve repair or replacement surgery

Exclusion Criteria

  • Patients undergoing concurrent surgical anti-arrythmia procedure
  • Heart transplant patients
  • Patients with known hematologic hypercoagulability disorder

Outcomes

Primary Outcomes

Incidence of Stroke

Time Frame: 4 years

Secondary Outcomes

  • Short- and Long-term biochemical parameters(1 and 5 years)
  • Short-term clinical outcomes (Procedural complications, hospital length of stay, etc)(30 days)

Study Sites (1)

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