NCT00766792CompletedNot Applicable
Removal of Uremic Toxins With Nocturnal Dialysis Versus Standard Dialysis
University Hospital, Ghent2 sites in 1 country15 target enrollmentStarted: December 2005Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University Hospital, Ghent
- Enrollment
- 15
- Locations
- 2
- Primary Endpoint
- To evaluate what is more effective for removal of uremic toxins - nocturnal versus standard dialysis?
Study Overview
Brief Summary
Dialysis patients, who decide to switch from standard dialysis (3 times 240-270 min/week) to nocturnal dialysis (3 times 480 min/week), will be followed. In parallel a control group with patients staying on standard dialysis will be followed. The study will last 30 weeks. During this period blood samples (pre- and post-dialysis: 10 times; inlet and outlet of dialyzer: 3 times) will be collected on predetermined time points. Concentration of several uremic retention solutes will be determined.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •age > 18 years
Exclusion Criteria
- •pregnancy
Outcomes
Primary Outcomes
To evaluate what is more effective for removal of uremic toxins - nocturnal versus standard dialysis?
Time Frame: 30 weeks
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (2)
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