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NCT00752583 Clinical Trial

Peritoneal Dialysis Versus Haemodialysis

Hemodialysis Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00752583
Other study ID # 2008/232
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 7, 2008
Est. completion date December 31, 2015

Study information
Verified date December 2022
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study in order to quantify toxin removal during dialysis

Recruitment information / eligibility
Status Completed
Enrollment 25
Est. completion date December 31, 2015
Est. primary completion date November 30, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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).

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Peritoneal dialysis
Blood, urine and dialysate sampling
• Haemodialysis
Blood, urine and dialysate sampling

Locations
Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Registration of toxin removal efficiency After 1 week and after 1, 3, 6, 9, 12, 18 and 24 months
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