Shin 1994.

Methods	Study design: cross‐over RCT Follow‐up period: 2 weeks Duration of study: not reported
Participants	Country: USA Setting: not reported Inclusion criteria: low pre‐HD BP or excessive interdialytic weight gain (details were unknown) Enrolled: 10 Age: not reported Sex (M/F): not reported Exclusion criteria: not reported
Interventions	Treatment arm 35°C dialysate Control arm 37°C dialysate
Outcomes	MAP during dialysis
Notes	Abstract‐only publication Funding source: not reported We requested further information but there was no response
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	Insufficient information to permit judgement: No description about the first phase data including missing values
Selective reporting (reporting bias)	Unclear risk	Insufficient information to permit judgement: 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