Methods |
Randomised clinical trial |
Participants |
186 participants 65 years of age or older undergoing elective unilateral total hip replacement
|
Interventions |
|
Outcomes |
Delirium, cerebrovascular accident, cardiac failure, myocardial infarction, pulmonary embolism, pneumonia, superficial wound infection, urinary tract infection, acute renal failure |
Notes |
‐ |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Low risk |
The trial used a random number table. |
Allocation concealment (selection bias) |
Low risk |
The trial used a sealed envelope technique. |
Blinding of participants and personnel (performance bias)
All outcomes |
Unclear risk |
The blinding of participants and personnel was not described. |
Blinding of outcome assessment (detection bias)
All outcomes |
Unclear risk |
The blinding of outcome assessment was not described. |
Incomplete outcome data (attrition bias)
All outcomes |
Low risk |
There was a low rate of missing data. |
Selective reporting (reporting bias) |
Low risk |
No reporting bias was apparent. |
Other bias |
Low risk |
No other bias was apparent. |