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Peritoneal Dialysis Versus Haemodialysis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00752583
Recruitment Status : Unknown
Verified December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
First Posted : September 15, 2008
Last Update Posted : December 5, 2014
Information provided by (Responsible Party):
University Hospital, Ghent

Brief Summary:
Study in order to quantify toxin removal during dialysis

Condition or disease Intervention/treatment Phase
Hemodialysis Procedure: Peritoneal dialysis Procedure: Haemodialysis Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 75 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Clinical Study in Order to Quantify Solute Removal in Peritoneal Dialysis Versus Haemodialysis
Study Start Date : September 2008
Estimated Primary Completion Date : May 2015
Estimated Study Completion Date : December 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dialysis

Arm Intervention/treatment
Experimental: 1
Peritoneal dialysis
Procedure: Peritoneal dialysis
Blood, urine and dialysate sampling

Active Comparator: 2
Procedure: Haemodialysis
Blood, urine and dialysate sampling

Primary Outcome Measures :
  1. Registration of toxin removal efficiency [ Time Frame: After 1 week and after 1, 3, 6, 9, 12, 18 and 24 months ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00752583

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Contact: Sunny Eloot, PhD

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University Hospital Ghent Recruiting
Ghent, Belgium, 9000
Principal Investigator: Raymond Vanholder, MD, PhD         
Sub-Investigator: Sunny Eloot, PhD         
Sponsors and Collaborators
University Hospital, Ghent
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Principal Investigator: Raymond Vanholder, MD, PhD University Hospital, Ghent
Additional Information:
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Responsible Party: University Hospital, Ghent Identifier: NCT00752583    
Other Study ID Numbers: 2008/232
First Posted: September 15, 2008    Key Record Dates
Last Update Posted: December 5, 2014
Last Verified: December 2014
Keywords provided by University Hospital, Ghent:
Chronic renal insufficiency (patients under dialysis)