Methods |
Study design: cross‐over RCT
Follow‐up period: 3 weeks
Duration of study: not reported
|
Participants |
|
Interventions |
Treatment arms
Dialysate at 37.8°C
Dialysate at 36.7°C
Dialysate at 35.6°C
|
Outcomes |
|
Notes |
|
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Unclear risk |
Study was described as randomised; method of randomisation was not reported |
Allocation concealment (selection bias) |
Unclear risk |
Insufficient information to permit judgement |
Blinding of participants and personnel (performance bias)
All outcomes |
High risk |
Blinding was not feasible because of the nature of the intervention |
Blinding of outcome assessment (detection bias)
All outcomes |
Unclear risk |
Insufficient information to permit judgement |
Incomplete outcome data (attrition bias)
All outcomes |
Unclear risk |
No description about the first phase data including missing values |
Selective reporting (reporting bias) |
Unclear risk |
The protocol was not available |
Other bias |
High risk |
Carry‐over effects potentially existed. No description for the assessment of the baseline imbalance of first period of the cross‐over study |