NCT01753154.

Methods	Study design: cross‐over RCT Randomisation method: not reported Blinding: open label Intention to treat: unclear Follow‐up period: 16 weeks
Participants	Countries: Poland and Spain Setting: multicentre prevalent APD patients
Interventions	Balance PD solution for 8 weeks then conventional PD solution for another 8 weeks
Outcomes	RRF Peritoneal UF Peritoneal solute clearance fluid status
Notes	Study recently completed; no data available