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Cohort Study Comparing Short Daily Hemodialysis (HD) With Conventional HD
This study is ongoing, but not recruiting participants.
Sponsors and Collaborators: Hamilton Health Sciences
Nephrology Divisional Research Funds, St. Joseph's Healthcare
Information provided by: McMaster University
ClinicalTrials.gov Identifier: NCT00182156
  Purpose

This study is examining the effects of short daily hemodialysis on platelet function, fluid volume control, arterial stiffness and patient quality of life, as compared to conventional hemodialysis.


Condition
End-Stage Renal Disease
Thrombocytopathy
Cardiovascular Diseases

MedlinePlus related topics: Dialysis Kidney Failure
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Cross-Sectional
Official Title: Cohort Study Examining the Effects of Short Daily Hemodialysis As Compared to Conventional Hemodialysis in Outpatients Treated at St Joseph's Healthcare, Hamilton

Further study details as provided by McMaster University:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 40
Study Start Date: October 2004
Estimated Study Completion Date: December 2008
Estimated Primary Completion Date: December 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
conventional HD
2
short daily HD
3
PD

Detailed Description:

Bleeding is a common cause of morbidity and mortality in patients with end stage renal disease. A major cause of uremic bleeding is due to platelet dysfunction. It has been theorized that in renal failure, toxins accumulate, some of which inhibit primary hemostasis. All aspects of normal platelet function are affected. Platelet function has previously been difficult to quantify but recently a novel test, the platelet function analyzer (PFA-100) has been determined to be both sensitive and specific in assessing platelet function. Conventional hemodialysis (CHD) has been shown to partially correct thrombocytopathy. Enhanced uremic clearance can now be attained through the use of short daily hemodialysis (SDHD). Cardiovascular disease is the most common cause of mortality in dialysis patients, accounting for 40% of deaths. Volume overload is associated with high blood pressure, left ventricular hypertrophy and elevated markers of inflammation and these factors have been associated with increased cardiovascular mortality. SDHD has been shown to control blood pressure and limit volume expansion. Pulse wave velocity (PWV) has been used to assess arterial compliance and reduction of arterial elasticity of large and small arteries which have been associated with cardiovascular outcomes.

  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

Short daily HD v PD v conventional HD

Criteria

Inclusion Criteria:

  • Patient is enrolled in short daily hemodialysis program
  • Patient is minimum of 18 years old

Exclusion Criteria:

  • Patient is unable to consent due to language barrier
  • Patient is unable to consent due to cognitive difficulties
  • Patient refuses consent
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00182156

Locations
Canada, Ontario
St. Joseph's Healthcare
Hamilton, Ontario, Canada, L8N 4A6
Sponsors and Collaborators
Hamilton Health Sciences
Nephrology Divisional Research Funds, St. Joseph's Healthcare
Investigators
Principal Investigator: Azim Gangji, MD Clinical Scholar, Medicine
Principal Investigator: Catherine M Clase, MD Associate Professor, Medicine
  More Information

Responsible Party: McMaster University ( Dr Azim Gangji )
Study ID Numbers: Nephrology Divisional Funds
Study First Received: September 10, 2005
Last Updated: June 16, 2008
ClinicalTrials.gov Identifier: NCT00182156  
Health Authority: Canada: Health Canada

Keywords provided by McMaster University:
hemodialysis
platelet function analyzer
bioimpedance
pulse wave velocity
end stage renal disease

Study placed in the following topic categories:
Thrombocytopathy
Renal Insufficiency
Urologic Diseases
Renal Insufficiency, Chronic
Hematologic Diseases
Blood Platelet Disorders
Kidney Failure, Chronic
Kidney Diseases
Kidney Failure

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 15, 2009