thrombosis prevention | versus placebo or control No demonstrated result for efficacy nadroparin inferior to placebo in terms of total bleeding in Pezzuoli, 1989 nadroparin inferior to placebo in terms of major Bleeding in Pezzuoli, 1989 nadroparin inferior to placebo in terms of wound hematoma in Pezzuoli, 1989 nadroparin inferior to placebo in terms of transfusin in Pezzuoli, 1989 | 2 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
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Pezzuoli, 1989 | nadroparin vs placebo | symptomatic thromboembolism event 0.29 [0.11; 0.80] | total bleeding 2.09 [1.80; 2.44] major Bleeding 2.51 [1.91; 3.30] wound hematoma 1.88 [1.55; 2.29] transfusin 1.65 [1.34; 2.03] | all cause death 0.45 [0.19; 1.02] Pulmonary embolism 0.25 [0.05; 1.18] | Roth, 1995 | nadroparin vs control | | | minor bleeding 5.00 [0.60; 41.55] VTE (symptomatic or asymptomatic) 0.20 [0.02; 1.66] symptomatic VTE 1.00 [0.06; 15.63] |
Trial | Treatments | Patients | Method |
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Pezzuoli, 1989 | Nadroparin 2850 anti-Xa units (n=2247) vs. Placebo (n=2251) | general surgery | Blind Sample size: 2247/2251 Primary endpoint: FU duration: | Roth, 1995 | 0.3 ml sc fraxiparine 2 hours before the operation and self administered daily (except the firstvtwo doses) for 4 days after surgeryn/x (n=61) vs. no treatment (n=61) | patients undergoing ambulatory arthroscopic | Parallel groups Sample size: 61/61 Primary endpoint: FU duration: 4 days |
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thrombosis prevention | versus Unfractionated heparin No demonstrated result for efficacy | 1 trial | meta-analysis | | Trial | control | p<0.05 | harm | NS |
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Leyvraz, 1991 | nadroparin vs Unfractionated heparin | | | |
Trial | Treatments | Patients | Method |
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Leyvraz, 1991 | Fraxiparin (n=203) vs. Unfractionated heparin (n=206) | Elective hip | Sample size: 203/206 Primary endpoint: FU duration: |
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