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See also:
All venous thrombosis clinical trials
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Treatments
Studied treatment |
continuation for 2 additionnal months of warfarin adjusted to achieve
a target INR between 2.0 and 3.0.
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Control treatment |
discontinuation (after 1 months)
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Patients
Inclusion criteria |
first episode of idiopathic venous thromboembolism; DVT demonstrated by bilateral compression ultrasonography of the proximal leg veins, and (if possible) bilateral impedance plethysmography; PE by ventilation-perfusion lung scan; |
Exclusion criteria |
other indications for, or contraindication to, long-termanticoagulant therapy; need for long-term treatment with nonsteroidal anti-inflammatory drugs, ticlopidine, sulfinpyrazone, dipyridamole, or more than 160 mg of aspirin per day; familial bleeding disorder; major psychiatric disorder; pregnant or could become pregnant |
Baseline characteristics |
time of randomization |
1 months |
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Method and design
Randomized effectives |
NA / NA (studied vs. control) |
Design |
Parallel groups |
Blinding |
double blind |
Follow-up duration |
11 months (after randomizatio) |
Number of centre |
13 |
Geographic area |
Canada, US |
Primary endpoint |
recurrent VTE |
Results
No results available for this trial
- no clinical endpoint reported
Reference(s)
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Kearon C, Ginsberg JS, Anderson DR, Kovacs MJ, Wells P, Julian JA, Mackinnon B, Demers C, Douketis J, Turpie AG, Van Nguyen P, Green D, Kassis J, Kahn SR, Solymoss S, Desjardins L, Geerts W, Johnston M, Weitz JI, Hirsh J, Gent M.
Comparison of 1 month with 3 months of anticoagulation for a first episode of venous thromboembolism associated with a transient risk factor..
J Thromb Haemost 2004;2:743-9
Pubmed
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