CClinicalTrials.gg
CompletedNCT00486915Updated Aug 15, 2019

Impact of Left Atrial Appendage Exclusion on Short-Term Clinical Outcomes and Long-Term Stroke Incidence

An interventional study of Left Atrial Appendage Ligation in Atrial Fibrillation, Thromboembolism and Cerebrovascular Accident, sponsored by London Health Sciences Centre. Completed at 1 site in Italy. Per ClinicalTrials.gov, last updated 2019-08-15.

Sponsored by London Health Sciences Centre · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
43
Allocation
Randomized
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Atrial Fibrillation
  • Thromboembolism
  • Cerebrovascular Accident

Keywords

  • Atrial Fibrillation
  • Left Atrial Appendage
  • Surgical Ligation
  • Thromboembolism
  • Cerebrovascular Accident
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 43 is below the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

London Health Sciences Centre is the lead sponsor of 39 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients undergoing mitral valve repair or replacement surgery

Exclusion criteria

Exclusion Criteria:

  • Patients undergoing concurrent surgical anti-arrythmia procedure
  • Heart transplant patients
  • Patients with known hematologic hypercoagulability disorder
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
43 participants (actual)

Study arms

  • Active comparator
    Left Atrial Appendage Exclusion

    Procedure: Left Atrial Appendage Ligation

  • No intervention
    Control

Interventions

  • ProcedureLeft Atrial Appendage Ligation
06

What researchers measure

Primary outcomes

  1. Incidence of Stroke

    Time frame: 4 years

Secondary outcomes

  1. Short- and Long-term biochemical parameters

    Time frame: 1 and 5 years

  2. Short-term clinical outcomes (Procedural complications, hospital length of stay, etc)

    Time frame: 30 days

07

Study locations

1 site
  • Hospital San Rafael
    Milan, MI, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 15, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00486915
Lead sponsor
London Health Sciences Centre
Collaborators
Ospedale San Raffaele
Responsible party
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) — Principal investigator
First posted
Jun 15, 2007
Start date
Apr 2007
Primary completion
Dec 2008
Completion
Dec 2012
Last update
Aug 15, 2019

Study contacts

Dave Nagpal, MD
principal investigator · London Health Sciences Centre
Lucia Torracca, MD
principal investigator · Hospital San Rafael
Ottavio Alfieri, MD
study director · Hospital San Rafael

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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