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Removal of Uremic Toxins With Nocturnal Dialysis Versus Standard Dialysis

G

Ghent University Hospital (UZ)

Status

Completed

Conditions

Chronic Renal Failure

Treatments

Procedure: Standard dialysis
Procedure: Nocturnal dialysis

Study type

Interventional

Funder types

Other

Identifiers

NCT00766792
2005/288

Details and patient eligibility

About

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.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age > 18 years

Exclusion criteria

  • pregnancy

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

15 participants in 2 patient groups

1
Experimental group
Description:
Nocturnal dialysis
Treatment:
Procedure: Nocturnal dialysis
2
Active Comparator group
Description:
Standard dialysis
Treatment:
Procedure: Standard dialysis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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