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Study identifier: NCT03994471 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of XyloCore Peritoneal Dialysis Solution.

Condition: End Stage Renal Disease  ·  Sponsor: Iperboreal Pharma Srl

PhasePhase 3
Planned participants170
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Randomized, controlled, parallel groups, open-label, blinded end-point assessment, multicenter study, comparing the effects of a low glucose peritoneal dialysis solution, XyloCore, to glucose solutions (Physioneal, Fixioneal, Dianeal, Balance, Bicavera, Bicanova or Equibalance) only regimen, in patients with End-Stage Renal Disease (ESRD) receiving Continuous Ambulatory Peritoneal Dialysis (CAPD), over a 6-month study period.

This description comes directly from the study's public registry record.

Talk to the study team

Arduino Arduini, MD  ·  +39.333.6409595  ·  a.arduini@iperboreal.com

Always discuss trial participation with your own doctor first.

Locations (41)

Aalborg UniversityAalborg, DenmarkNot Yet Recruiting
Aarhus University HospitalAarhus, DenmarkRecruiting
Zealand University HospitalRoskilde, DenmarkRecruiting
Dialysis Center DaVitaDüsseldorf, GermanyRecruiting
Ospedale Madonna del SoccorsoAscoli Piceno, ItalyRecruiting
Ospedale Santa Maria AnnunziataBagno a Ripoli, ItalyNot Yet Recruiting
Azienda Universitaria Ospedaliera di BariBari, ItalyRecruiting
ASST Spedali Civili di BresciaBrescia, ItalyNot Yet Recruiting
Ospedale SS. AnnunziataChieti, ItalyRecruiting
IRCCS Policlinico San MartinoGenova, ItalyNot Yet Recruiting
Ospedale Civile San SalvatoreL’Aquila, ItalyRecruiting
ASST Fatebenefratelli-Sacco -Ospedale Luigi SaccoMilan, ItalyRecruiting

+ 29 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT03994471