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. 2016 Jul 15;2016(7):CD001893. doi: 10.1002/14651858.CD001893.pub2

Dauri 2003.

Methods RCT
Written informed consent obtained
Setting: Italy
Funding: unspecified
Participants 25 patients undergoing cadaveric renal transplantation
Interventions Treatment group: TEA (T12‐L1) with ropivacaine 0.2% and fentanyl 2 mcg/mL for 24 hours (n = 13)
Control group: IV tramadol (n = 12)
Outcomes VAS at rest at 6 and 24 hours
VAS on movement at 6 and 24 hours
Hospital LOS
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk "randomly allocated into two groups", no details
Allocation concealment (selection bias) Unclear risk Not mentioned
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk Not mentioned
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk Not mentioned
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No loss to follow‐up mentioned
Selective reporting (reporting bias) Low risk All results reported
Other bias Low risk Groups well balanced