Peritoneal Dialysis Versus Haemodialysis

• Sponsor: University Hospital, Ghent (Other)
• Overall Status: Unknown status
• CT.gov ID: NCT00752583
• Collaborator: (none)
• Enrollment: 75
• Location: 1
• Arms: 2
• Duration (Months): 87
• Patients Per Site Per Month: 0.9

Study Details

Study Description

Brief Summary

Study in order to quantify toxin removal during dialysis

Condition or Disease	Intervention/Treatment	Phase
Hemodialysis	Procedure: Peritoneal dialysis; Procedure: Haemodialysis	N/A

Study Design

• Study Type: Interventional
• Anticipated 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: Sep 1, 2008
• Anticipated Primary Completion Date: May 1, 2015
• Anticipated Study Completion Date: Dec 1, 2015

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 1 Peritoneal dialysis	Procedure: Peritoneal dialysis; Blood, urine and dialysate sampling
Active Comparator: 2 Haemodialysis	Procedure: Haemodialysis; Blood, urine and dialysate sampling

Outcome Measures

Primary Outcome Measures

1. Registration of toxin removal efficiency [After 1 week and after 1, 3, 6, 9, 12, 18 and 24 months]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• 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).

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University Hospital Ghent	Ghent		Belgium	9000

Sponsors and Collaborators

• University Hospital, Ghent

Investigators

• Principal Investigator: Raymond Vanholder, MD, PhD, University Hospital, Ghent

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• Website of the University Hospital Ghent

Publications

None provided.

• Responsible Party: University Hospital, Ghent
• ClinicalTrials.gov Identifier: NCT00752583
• Other Study ID Numbers: 2008/232
• First Posted: Sep 15, 2008
• Last Update Posted: Dec 5, 2014
• Last Verified: Dec 1, 2014

• Keywords provided by University Hospital, Ghent: Chronic renal insufficiency (patients under dialysis)

Study Results

No Results Posted as of Dec 5, 2014