Yang 2002b.

Methods	Study design: cross‐over RCT Randomisation method: not reported Blinding: open label Intention to treat: unclear Follow‐up period: 8 weeks
Participants	Countries: Taiwan Setting: single centre Prevalent CAPD patients
Interventions	Received either 7.5% icodextrin or 2.5% dextrose for the overnight dwell for 28 days and then cross‐over for another 28 days
Outcomes	UF 4‐hour dialysate:plasma creatinine BP
Notes	Unable to obtain data from the first phase of cross‐over study

APD ‐ automated peritoneal dialysis; BP ‐ blood pressure; CAPD ‐ continuous ambulatory peritoneal dialysis; CrCl ‐ creatinine clearance; CRP ‐ C‐reactive protein; GDP ‐ glucose degradation products; ECG ‐ echocardiogram; PD ‐ peritoneal dialysis; RCT ‐ randomised controlled trial; RRF ‐ residual renal function; UF ‐ ultrafiltration