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Effect of rHDL on Atherosclerosis - Safety and Efficacy: THE ERASE TRIAL
This study has been completed.
Sponsored by: CSL Limited
Information provided by: CSL Limited
ClinicalTrials.gov Identifier: NCT00225719
  Purpose

Currently available therapies to treat Acute Coronary Syndromes(ACS) have several limitations including; the relatively long treatment duration required before apparent significant benefit; the inability to achieve reversal of the atherosclerotic process; and poor patient compliance due to chronicity of therapy. This study will assess the effects of rHDL compared with placebo on indices of atherosclerosis progression and regression as assessed with intravascular ultrasound (IVUS) in patients after acute coronary syndromes (ACS).


Condition Intervention Phase
Acute Coronary Syndromes
Drug: rHDL
Phase II

MedlinePlus related topics: Ultrasound
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Regression of Coronary Atherosclerotic Lesions After rHDL Infusions in Acute Coronary Syndrome Patients as Assessed by Intravascular Ultrasound.

Further study details as provided by CSL Limited:

Primary Outcome Measures:
  • Efficacy

Secondary Outcome Measures:
  • Safety

Estimated Enrollment: 180
Study Start Date: July 2005
  Eligibility

Ages Eligible for Study:   30 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female 30 - 75 years of age
  • Recent acute coronary syndrome, defined as unstable angina, non-Q wave myocardial infarction, or ST elevation indicative of myocardial infarction, within the last 14 days

Exclusion Criteria:

  • >50% stenosis by visual angiographic estimation in the left main artery
  • Renal insufficiency
  • Severe liver disease
  • Congestive heart failure as defined by the NYHA classification as functional Class III or Class IV
  • Previous or planned coronary artery bypass surgery
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00225719

Locations
Canada, Quebec
Montreal Heart Institute
Montreal, Quebec, Canada, H1T 1C8
Sponsors and Collaborators
CSL Limited
Investigators
Principal Investigator: Jean-Claude Tardif, MD FRCP Montreal Heart Institute
  More Information

Publications indexed to this study:
Responsible Party: CSL Limited ( Dr Russell Basser )
Study ID Numbers: CSLCT-HDL-04-06
Study First Received: September 23, 2005
Last Updated: November 6, 2008
ClinicalTrials.gov Identifier: NCT00225719  
Health Authority: Canada: Health Canada

Study placed in the following topic categories:
Atherosclerosis
Heart Diseases
Myocardial Ischemia
Acute Coronary Syndrome
Vascular Diseases
Ischemia

Additional relevant MeSH terms:
Pathologic Processes
Disease
Syndrome
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009