Skip to main content
Clinical Trials/NCT00563355
NCT00563355
Completed
N/A

A Prospective Randomised Controlled Trial to Study the Effects of Recombinant Human Erythropoietin on the Progression of Atherosclerosis, Cardiovascular Function, Nutrition and Residual Renal Function in Pre-dialysis Chronic Renal Failure Patients

Hospital Authority, Hong Kong1 site in 1 country66 target enrollmentFebruary 2001

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Disease
Sponsor
Hospital Authority, Hong Kong
Enrollment
66
Locations
1
Primary Endpoint
endothelial function and atherosclerosis
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The primary aim of the study is to evaluate the effects of correction of anemia using erythropoietin on the progression of atherosclerosis and cardiac muscle thickening in patients with chronic kidney disease

Registry
clinicaltrials.gov
Start Date
February 2001
End Date
November 2003
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Authority, Hong Kong

Eligibility Criteria

Inclusion Criteria

  • Patients with chronic renal failure with serum creatinine between 150umol/L and 800umol/L and at the same time Hb
  • Patients with regression line of 1/serum creatinine versus time showing that they may not require dialysis within the coming 12 months
  • Patients below the age of 75

Exclusion Criteria

  • Patients with valvular heart disease/congenital heart disease
  • Patients with ischemic heart disease/history of myocardial infarction/coronary artery bypass surgery
  • Patients with history of heart failure
  • Patients with regression line of 1/serum creatinine versus time showing that the estimated date of end stage renal disease is within 12 months
  • Patients with thalassemic trait or haemoglobinopathies
  • Patients with underlying haematological malignancies
  • Patients with active bleeding
  • Patients with uncorrected iron or other vitamins deficiencies
  • Patients with poor general condition

Outcomes

Primary Outcomes

endothelial function and atherosclerosis

Time Frame: 6 month, 1 year

cardiac hypertrophy and cardiac function

Time Frame: 6 month, 1 year

Secondary Outcomes

  • nutrition status(6 month, 1 year)
  • residual renal function(6 month, 1 year)
  • quality of life(6 month, 1 year)

Study Sites (1)

Loading locations...

Similar Trials