Kakkar 1969.
| Methods | Allocation: random Single blind Exclusions after randomisation: 2 Losses to follow‐up: nil |
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| Participants | Country: UK Participants: 30 Age: 18 to 77 years Sex: Male and female Inclusion criteria: venographically confirmed DVT of leg duration < 4 days Exclusion criteria: surgery < 3 days; unhealed wound; peptic ulcer; diastolic BP > 100 mmHg |
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| Interventions | Treatment: (2 groups) streptokinase 500,000 U IV over 30 minutes, 900,000 U every 6 hours for 5 days or (Arwin) 80 U in 6 hours, then 80 units in 15 minutes, then 40 ‐ 80 U every 6 hours for 5 days Control: heparin 10,000 U over 5 minutes, then 10,000 to 15,000 U every 6 hours for 5 days Co‐treatment: oral anticoagulation commenced at end of infusions. Bed rest, leg elevation, bandages to all groups |
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| Outcomes | 1 month: mortality; PE; clot lysis; bleeding 6 to 12 months: clot lysis after partial lysis |
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| Notes | 1 excluded as died of PE in heparin group. 1 excluded due to bleeding in streptokinase group Included 7 patients with tibial vein thrombosis only (4 heparin, 2 streptokinase, 1 Arwin) |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | description not clear |
| Allocation concealment (selection bias) | Unclear risk | description not clear |
| Blinding of participants and personnel (performance bias) All outcomes | High risk | not described |
| Blinding of outcome assessment (detection bias) All outcomes | High risk | not described |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | no missing data |
| Selective reporting (reporting bias) | Low risk | all outcomes reported |
| Other bias | Low risk | none |