Effectiveness of Bridging Anticoagulation for Surgery (The BRIDGE Study)
Completed · Phase 3 · Has a placebo group
Conditions studied: Arterial Thromboembolic Events, Atrial Fibrillation
In brief
Blood thinners, such as warfarin, prevent blood clots from forming, thereby reducing the risk of a stroke or heart attack. When people undergo surgery or certain procedures, they must stop using warfarin to prevent too much bleeding during and after the surgery or procedure. Some doctors prescribe a different blood thinner, one that works more quickly and wears off more quickly, to bridge the gap between starting and stopping warfarin. However, this short-term treatment is expensive, may increase the risk of bleeding, and has not been proven effective. This study will determine whether a bridging blood thinner called dalteparin is helpful or harmful for people with atrial fibrillation who stop taking warfarin in preparation for surgery or a procedure.
Key facts
- Study ID
- NCT00786474
- Run by
- Duke University
- People needed
- 1884
- Starts
- 2009-07-01
- Expected to finish
- 2015-02-01
- Last updated by the study team
- 2016-03-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Receiving warfarin therapy for at least 3 months, administered to achieve an international normalized ratio (INR) range of 2.0 to 3.0
- Requiring temporary interruption of warfarin for pre-specified elective procedure or surgery
- Presence of one of the following conditions:
- Chronic (permanent or paroxysmal) nonvalvular atrial fibrillation, confirmed by at least one prior electrocardiography recording or pacemaker or acid citrate dextrose (ACD) interrogation
- Chronic (permanent or paroxysmal) valvular atrial fibrillation with evidence of mitral valvular heart disease, confirmed by the same criteria as nonvalvular atrial fibrillation
- Presence of at least one of the following major stroke risk factors:
- Older than 75 years of age
- Hypertension
- Diabetes mellitus
- Congestive heart failure or left ventricular dysfunction
- Previous ischemic stroke, systemic embolism, or transient ischemic attack (TIA)
You may not qualify if…
- Any mechanical prosthetic heart valve
- Stroke (ischemic or hemorrhagic), systemic embolism, or TIA within the past 12 weeks
- Venous thromboembolism (deep vein thrombosis and/or pulmonary embolism) within past 12 weeks
- Major bleeding within the past 6 weeks
- Severe renal insufficiency, measured through a calculated creatinine clearance of less than 30 mL/min
- Thrombocytopenia
- Life expectancy less than 1 month
- Condition that impairs compliance with trial protocol, such as cognitive impairment, an uncontrolled psychiatric condition, or geographic inaccessibility
- Pregnancy
- Allergy to heparin or history of heparin-induced thrombocytopenia
- Having one of the following surgeries or procedures during warfarin interruption:
- Cardiac surgery, such as coronary artery bypass or heart valve replacement
- Neurosurgery that is intracranial or intraspinal, such as tumor resection or aneurysm repair
- High-risk non-surgical procedures, such as brain biopsy
- Other surgical or non-surgical procedure that, at the discretion of the surgeon, precludes administration of therapeutic-dose low molecular weight heparin (LMWH) at any time in the post-procedure period
- More than one surgery planned during the trial period
- Prior participation in this trial
Where it is running
- Duke Clinical Research Institute — Durham, North Carolina, United States
Full record on ClinicalTrials.gov
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