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Twelve patients who were enrolled after a diagnosis of 1st unprovoked proximal deep-vein thrombosis and who were included in the analysis were subsequently discovered to become ineligible after an assessment of the information: 8 were found not to experienced proximal deep-vein thrombosis, 2 got a provoked venous thromboembolism, 1 in the placebo group had a sign for long-term anticoagulation, and 1 in the aspirin group had got a prior unprovoked venous thromboembolism. The baseline features of the patients didn’t differ significantly between your two groups . A total of 447 patients signed up for the ASPIRE study were males, the median age was 54 years, 36 percent got a BMI of 30 or more, 15 percent reported that a first-degree relative had got a venous thromboembolism, 5 percent had a prior provoked venous thromboembolism, and 2 percent experienced active malignancy during randomization.