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Sponsored by: |
University of Turku |
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Information provided by: | University of Turku |
ClinicalTrials.gov Identifier: | NCT00479362 |
There are no established guidelines regarding interruption of warfarin anticoagulant therapy prior to surgical implantation of cardiac pacemakers.
Continuing the anticoagulant could potentially result in increased bleeding complications from the implantation surgery, whereas discontinuing the anticoagulant could predispose the patient to blood clots and strokes. In this study we intend to randomly assign warfarin-treated patients either into interrupted or continued warfarin therapy prior to pacemaker implantation with the purpose of establishing the rate of complication in these groups. Our hypothesis is that a cardiac pacing device can be safely implanted without discontinuation of the anticoagulant therapy.
Condition | Intervention | Phase |
---|---|---|
Hemorrhage Thrombosis Embolism |
Drug: Warfarin Drug: Aspirin Device: Permanent pacemaker Device: Implantable Cardioverter-defibrillator |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Safety Study |
Official Title: | Randomized Trial of Uninterrupted Versus Interrupted Anticoagulant Therapy in Patients Undergoing Cardiac Pacing Device Implantation |
Estimated Enrollment: | 400 |
Study Start Date: | September 2005 |
Estimated Study Completion Date: | July 2008 |
Despite greatly increased utilization of pacemaker and internal cardioverter-defibrillator (ICD) therapy for various indications in recent years, there are relatively few published studies on bleeding complications associated with the implantation of these devices. The purpose of our study is to assess the incidence and severity of hemorrhagic complications resulting from pacemaker and ICD implantation in patients treated with oral anticoagulant warfarin or acetyl salicylic acid.
There are no unified guidelines regarding warfarin use during pacemaker implantation. A case by case approach is commonly employed regarding whether to interrupt or to continue anticoagulant therapy prior to the procedure. Interrupting the therapy may expose the patient to thromboembolic complications, whereas continuing it can increase the risk of perioperative bleeding. Thus, either approach could potentially increase patient morbidity and prolong the hospital stay. Therefore, an evidence based choice of an appropriate approach in preparing the anticoagulant-treated patients for pacemaker implantation could have significant impact on both patient safety and over-all procedural cost.
We intend to assess the rate of hemorrhagic and thrombotic complications as well as the length of hospital stay associated with pacemaker or ICD implantation in patients randomized either to continue or to interrupt their warfarin treatment. One control group will be formed of pacemaker-receiving patients on acetyl salicylic acid as well as one group of patients on no medications affecting the coagulation system or thrombocyte aggregation.
Potential risk factors for bleeding or thromboembolic complications will be searched.
A total of 400 patients will be recruited into this multicenter study conducted at five hospitals in Finland. Warfarin users (n=200) will be randomly allocated into two groups: A. uninterrupted warfarin therapy maintained at accepted intensity (INR 2 to 3), and B. interruption of warfarin 2 days prior to device implantation. Control groups will comprised as described above with one hundred patients in each. The end-points of the study are: occurrences of major bleeding, haemorrhages and hematomas at pacemaker pocket, utilization of adjunctive therapies to control bleeding (e.g. Vitamin K or Fresh frozen plasma), need for surgical wound revision and thromboembolic complications. The duration of hospital stay will also be recorded. At two of the centres (Turku University Hospital and Satakunta Central Hospital) all patients will also be randomly assigned into two groups in which the implantation procedure will either be or not be guided by venous angiography.
Patients willing to participate in the study will receive both verbal and written information on the study and they will be asked to sign an informed consent. All devices will be implanted in a normal fashion according to generally accepted clinical guidelines. A variety of clinical and laboratory variables will be recorded in each study group to identify risk factors for bleeding and thromboembolism.
The aims of our study are to establish among patients implanted with pacemakers (1) whether uninterrupted warfarin therapy will increase the rate and severity of bleeding complications, (2) whether interruption of warfarin results in increased thromboembolic events, (3) whether aspirin treatment increases bleeding complications compared, and we also seek to identify factors predisposing to haemorrhagic complications.
Our main hypothesis is that a cardiac pacing device can be safely implanted without discontinuation of the anticoagulant therapy.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Petri Korkeila, MD | 358-50-3639710 | petri.korkeila@tyks.fi |
Finland | |
Turku University Hospital | Recruiting |
Turku, Finland, 20521 | |
Contact: Petri Korkeila, MD 358503639710 petri.korkeila@tyks.fi | |
Principal Investigator: Petri Korkeila, MD |
Study Director: | Juhani Airaksinen, MD | University of Turku, Turku University Hospital |
Principal Investigator: | Petri Korkeila, MD | Turku University Hospital |
Study ID Numbers: | TAHD-VARF |
Study First Received: | May 25, 2007 |
Last Updated: | May 25, 2007 |
ClinicalTrials.gov Identifier: | NCT00479362 History of Changes |
Health Authority: | Finland: Ethics Committee |
Pacemaker Cardioverter-defibrillator Hemorrhage |
Hematoma Thrombosis Embolism |
Hematoma Embolism and Thrombosis Anticoagulants Aspirin Embolism |
Vascular Diseases Warfarin Hemorrhage Thrombosis |
Embolism and Thrombosis Anticoagulants Pathologic Processes Embolism Therapeutic Uses Hematologic Agents |
Vascular Diseases Cardiovascular Diseases Hemorrhage Pharmacologic Actions Thrombosis |