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WithdrawnNCT00182156Updated Apr 15, 2022

Cohort Study Comparing Short Daily Hemodialysis (HD) With Conventional HD

An observational study in End-stage Renal Disease, Thrombocytopathy and Cardiovascular Diseases, sponsored by McMaster University. Withdrawn at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-04-15.

Sponsored by McMaster University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • End-stage Renal Disease
  • Thrombocytopathy
  • Cardiovascular Diseases

Keywords

  • hemodialysis
  • platelet function analyzer
  • bioimpedance
  • pulse wave velocity
  • end stage renal disease
03

In context

Kidney Diseases

3,840 studies on the registry are indexed under Kidney Diseases; 500 are open to participants now.

Browse Kidney Diseases studies →

Lead sponsor

McMaster University is the lead sponsor of 720 studies on the registry; 124 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Short daily HD v PD v conventional HD

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • Patient is unable to consent due to language barrier
  • Patient is unable to consent due to cognitive difficulties
  • Patient refuses consent
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
0 participants (actual)

Groups and cohorts

  • 1

    conventional HD

  • 2

    short daily HD

  • 3

    PD

06

Study locations

1 site
  • St. Joseph's Healthcare
    Hamilton, Ontario L8N 4A6, Canada
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 15, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00182156
Lead sponsor
McMaster University
Collaborators
St. Joseph's Healthcare Hamilton
Responsible party
Azim Gangji (Associate professor, McMaster University) — Principal investigator
First posted
Sep 16, 2005
Start date
Oct 2004
Primary completion
Dec 2008 (estimated)
Completion
Dec 2008 (estimated)
Last update
Apr 15, 2022

Study contacts

Azim Gangji, MD
principal investigator · Clinical Scholar, Medicine
Catherine M Clase, MD
principal investigator · Associate Professor, Medicine

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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