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OpenTrials
Completed

NCT Number: NCT00752583

Peritoneal Dialysis Versus Haemodialysis

Study in order to quantify toxin removal during dialysis

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Substudy 1: includes new starting dialysis patients on peritoneal dialysis PD or haemodialysis HD
  • Substudy 2: stabile haemodialysis patients and peritoneal dialysis patients. Patients will be matched for gender, time on dialysis, diabetes, renal function at the start of dialysis.
  • Substudy 3: patients on CAPD (continuous ambulant PD) or CCPD (continuous cyclic PD).

Treatment and study plan

Peritoneal dialysis

Procedure

Blood, urine and dialysate sampling

Haemodialysis

Procedure

Blood, urine and dialysate sampling

Primary outcomes

  1. Registration of toxin removal efficiency

    Time frame: After 1 week and after 1, 3, 6, 9, 12, 18 and 24 months

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Registry information

Official study title

Clinical Study in Order to Quantify Solute Removal in Peritoneal Dialysis Versus Haemodialysis

Important dates

Study start
2008
Primary completion
2015
Study completion
2015
First posted
Sep 15, 2008
Registry last updated
Dec 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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