Sadeghi 2007.
Methods | Prospective, randomised, double blinded study | |
Participants | Population: 67 patients undergoing hip fracture surgery Setting: Iran Date the study was conducted: 2004‐2005 |
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Interventions | Intervention: tranexamic acid single bolus dose of 15 mg kg–1 administered intravenously at induction of anaesthesia Control: the same volume of saline solution was infused |
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Outcomes | Blood loss, blood transfusion, thrombotic complications and neurological deficits. | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: Patients were randomised using a random number technique |
Allocation concealment (selection bias) | Low risk | Quote: The correct treatment option was assured by means of coded infusion syringes prepared by hospital pharmacy not involved otherwise in the study |
Blinding of outcome assessment (detection bias) Mortality | Low risk | Quote: Caring personnel both the staff of the operating room and the intensive care unit (ICU) were blinded regarding the type and nature of treatment |
Blinding of outcome assessment (detection bias) Transfusion | Low risk | Quote: Caring personnel both the staff of the operating room and the intensive care unit (ICU) were blinded regarding the type and nature of treatment |
Blinding of outcome assessment (detection bias) Complications | Low risk | Quote: Caring personnel both the staff of the operating room and the intensive care unit (ICU) were blinded regarding the type and nature of treatment |
Incomplete outcome data (attrition bias) Mortality | Unclear risk | Not reported |
Incomplete outcome data (attrition bias) Transfusion | Unclear risk | Not reported |
Incomplete outcome data (attrition bias) Complication | Unclear risk | Not reported |
Selective reporting (reporting bias) | Unclear risk | No protocol available |
Other bias | Unclear risk | ‐ |