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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01396863
Other study ID # VEK20100228
Secondary ID
Status Completed
Phase N/A
First received July 13, 2011
Last updated March 21, 2012
Start date July 2011
Est. completion date February 2012

Study information

Verified date March 2012
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection AgencyDenmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

The proposed controlled, randomized study aims to compare pre-dilution hemodiafiltration (HDF) and low flux hemodialysis (HD) regarding acute changes in the brain.

The study consist of two examination days placed one week apart. 12 HD patients will be recruited to the study. The patients will be randomly placed in two groups: Pre-dilution hemodiafiltration during the first examination and low flux hemodialysis during the second day or vice versa.

Brain Magnetic Resonance Imaging (MRI) will be obtained before and after both treatments. The MRI-data will later be processed to estimate brain volume changes during the two types of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age = 18 years

- Informed consent

- Patient with end-stage renal disease (ESRD)

- Stabile hemodialysis treatment (Kt/V = 1.3)

- No contraindications against MRI (pacemaker or other metal implants, claustrophobia, severe adiposity)

- Weight <140kg

Exclusion Criteria:

- Clinical signs of new structural, thromboembolic or vascular brain disease the last 3 month before entering the study

- Changes in corticosteroid treatment during the last two weeks

- Change in diuretics during the last two weeks

- Non-compliant with regard to salt and fluid intake

- Acute disease

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
HDF during the first examination
The patient will receive treatment with pre-dilution hemodiafiltration during the first examination. During the second examination the patient will receive treatment with low flux hemodialysis. MRI of the brain will be performed before and after the treatment. The MRI-data will later be processed to determine the degree of brain volume change due to the treatment.
HD during the first examination
The patient will receive treatment with low flux hemodialysis during the first examination. During the second examination the patient will receive treatment with pre-dilution hemodiafiltration. MRI of the brain will be performed before and after the treatment. The MRI-data will later be processed to determine the degree of brain volume change due to the treatment.

Locations

Country Name City State
Denmark Department of Renal Medicine C, Aarhus University Hospital, Skejby Aarhus N
Denmark The MR-Research Centre, Aarhus University Hospital, Skejby Aarhus N

Sponsors (2)

Lead Sponsor Collaborator
University of Aarhus The Danish Medical Research Council

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Brain Volume Change (PBVC) Brain volume before and after one hemodialysis session (4,5 hours) and one session of hemodiafiltration (4,5 hours). Dialysis sessions are performed one week apart. Randomization determines the order of treatment (hemodialysis vs hemodiafiltration).
MRI-data will later be processed to estimate the PBVC.
Brain volume before and after one hemodialysis session (4,5 hours) and one session of hemodiafiltration (4,5 hours). Dialysis sessions are performed one week apart. No
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