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The Interrelation of the Vasculature, Endothelium, Bone Metabolism and Uremic Toxins in Peritoneal Dialysis (INVEST-PD)
This study is currently recruiting participants.
Verified by Universitaire Ziekenhuizen Leuven, March 2008
Sponsored by: Universitaire Ziekenhuizen Leuven
Information provided by: Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier: NCT00433264
  Purpose

Despite major advances in the treatment of chronic kidney disease, the age and sex matched mortality far exceeds that of the normal population. As in the normal population, the majority of deaths are related to cardiovascular disease. Mounting data point to the lethal synergy between chronic kidney disease and cardiovascular disease. This relation is present from early stages of chronic kidney disease on.

Several uremic toxins have been demonstrated to play an important role in kidney disease related endothelial dysfunction. In peritoneal dialysis patients, data on the relation between uremic toxins, endothelial dysfunction and microparticles are lacking.

We hypothesise that endothelial dysfunction and uremic toxins are interrelated in peritoneal dialysis patients


Condition Intervention Phase
Chronic Kidney Disease
Procedure: peritoneal dialysis
Phase 0

MedlinePlus related topics: Kidney Failure
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: The Interrelation of the Vasculature, Endothelium, Bone Metabolism and Uremic Toxins in Peritoneal Dialysis

Further study details as provided by Universitaire Ziekenhuizen Leuven:

Biospecimen Retention:   Samples With DNA

Biospecimen Description:

serum, plasma, DNA


Estimated Enrollment: 60
Study Start Date: February 2007
Estimated Study Completion Date: December 2008
Intervention Details:
    Procedure: peritoneal dialysis
    individualised
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Tertiary referral center university hospital

Criteria

Inclusion Criteria:

  • age > 18
  • Maintenance peritoneal dialysis

Exclusion Criteria:

  • No informed consent
  • Peritonitis
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00433264

Contacts
Contact: Björn Meijers, MD +32 16 342352 bjorn.meijers@uz.kuleuven.ac.be
Contact: Kathleen Claes, MD + 32 16 344580 kathleen.claes@uz.kuleuven.ac.be

Locations
Belgium, Vlaams-Brabant
Universitaire Ziekenhuizen Leuven Recruiting
Leuven, Vlaams-Brabant, Belgium, 3000
Contact: Bjorn Meijers, MD     +32 16 342352     bjorn.meijers@uz.kuleuven.ac.be    
Contact: Kathleen Claes, MD     +32 16 344580     kathleen.claes@uz.kuleuven.ac.be    
Principal Investigator: Bjorn Meijers, MD            
Principal Investigator: Kathleen Claes, MD            
Sponsors and Collaborators
Universitaire Ziekenhuizen Leuven
Investigators
Principal Investigator: Bjorn Meijers, MD UZ Leuven
Principal Investigator: Kathleen Claes, MD UZ Leuven
Study Director: Pieter Evenepoel, MD, PhD UZ Leuven
  More Information

Responsible Party: University Hospitals Leuven ( Pieter Evenepoel )
Study ID Numbers: ML3645
Study First Received: February 7, 2007
Last Updated: March 12, 2008
ClinicalTrials.gov Identifier: NCT00433264  
Health Authority: Belgium: Institutional Review Board

Keywords provided by Universitaire Ziekenhuizen Leuven:
peritoneal dialysis
endothelium
endothelial dysfunction

Study placed in the following topic categories:
Renal Insufficiency
Urologic Diseases
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Kidney Diseases
Kidney Failure

ClinicalTrials.gov processed this record on January 16, 2009