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Study of Intravenous Amino Acid Infusion to Prevent Contrast Dye Mediated Renal Damage

Primary Purpose

Contrast Nephropathy, Renal Failure

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Amino Acid
Placebo
Sponsored by
Queen's University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Contrast Nephropathy focused on measuring contrast nephropathy, renal failure, Travasol

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Greater then 18 years of age Referral for coronary angiography Type 1 or type 2 diabetic requiring insulin or oral hypoglycemic agents Stable serum creatinine concentration (140 to 300 μmol per liter for men or 125 to 300 μmol per liter for women or a creatinine clearance not greater than 60 ml/min (as calculated by Cockcroft-Gault equation) Non diabetic subjects with a stable serum creatinine concentration of 160 to 300 µmol per liter for men and 140 to 300 µmol per liter for women. Stable renal function defined as no documented rise or fall in serum creatinine by more then 44 umol/L in the preceding 2 weeks Exclusion Criteria: Refusal or inability to give consent Pregnant Non-elective coronary angiography Recent administration (within 21 days) of iodinated intravenous contrast dye Recent administration (within 21 days) of non-steroidal anti-inflammatory drugs (excluding aspirin), aminoglycoside antibiotics or chemotherapeutic agents Severe/unstable diabetics requiring emergency room or inpatient therapy in the previous 21 days Compensated or decompensated hepatic failure Renal transplant

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    1

    2

    Arm Description

    Intravenous saline infusion plus amino acid infusion

    Intravenous saline infusion plus placebo infusion

    Outcomes

    Primary Outcome Measures

    to assess if the infusion of amino acids will help prevent kidney damage that can occur when angiographic dye is used to perform a cardiac catheterization

    Secondary Outcome Measures

    the serum cystatin C level at 24 hours post procedure and 72 hours post procedure
    the number of patients with a peak increase in serum creatinine concentration of at least 44.1 umol/L between day 0 and day 3 (72 hours)
    the number of patients with a peak increase in serum creatinine concentration of at least 88.4 μmol per liter between day 0 and day 3 (72 hours) post-catheterization
    development of heart failure or myocardial infarction within 7 days
    need for renal replacement therapy
    death at 48 hours, 7 days, or 14 days post-catheterization
    number of hospital days after catheterization

    Full Information

    First Posted
    April 11, 2006
    Last Updated
    March 10, 2015
    Sponsor
    Queen's University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00313807
    Brief Title
    Study of Intravenous Amino Acid Infusion to Prevent Contrast Dye Mediated Renal Damage
    Official Title
    CoNTRST - Contrast Nephropathy and Travasol for Renal Safety Trial: Intravenous Amino Acid Infusion for the Prevention of Contrast-mediated Acute Renal Failure Following Coronary Catheterization
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Abandoned due to lack of recruitment Oct 2006
    Study Start Date
    November 2005 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    September 2008 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Queen's University

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Exposure to radiographic contrast dye during coronary angiography is well known to cause either transient decreases in renal function or acute renal failure. Although the overall incidence is low, acute renal failure occurs most frequently in patients with both diabetes and chronic renal failure where the average reported incidence is upwards of 20%. The etiology of contrast-induced nephropathy is related to acute decline in renal blood flow following dye exposure resulting in ischemic injury at the level of the medulla. The development of acute renal failure following radiocontrast dye administration is significant because it contributes to morbidity and mortality in patients at risk. The administration of amino acids, either through intravenous infusion or a protein meal, results in a substantial increase in renal plasma flow (RPF) and glomerular filtration rate (GFR). In both healthy subjects and in those with chronic renal failure, an amino acid infusion produces a 20% rise in GFR and effective RPF. We hypothesize that the 20% rise in effective RPF and GFR following an amino acid infusion will counteract the radiocontrast dye-induced vasoconstriction and reduce the renal toxicity of contrast medium in a group of high-risk patients.
    Detailed Description
    Exposure to radiographic contrast dye during coronary angiography is well known to cause either transient decreases in renal function or acute renal failure. Retrospective studies have confirmed that at least 60% of contrast-associated nephropathy occurs in subjects with chronic renal failure. The incidence approaches 20% in those with a baseline creatinine greater than 198.2 μmol per liter (2.25 mg/dL). Diabetes, in the absence of renal insufficiency, does not appear to confer added risk; however diabetic patients with chronic renal failure are at highest risk. It is particularly this group that develops oliguric renal failure requiring temporary or permanent renal replacement therapy. In diabetic patients with mild to moderate renal failure, the incidence of contrast-associated nephropathy has been reported to be between 9% and 40% however a greater then 50% incidence has been noted in diabetic patients with more severely impaired renal function. It is hypothesized that the renal toxicity of contrast medium is related to local vasoconstriction. We hypothesize that the protein-stimulated rise in effective RPF and GFR might counteract this intrarenal vasoconstriction and reduce the toxicity of contrast medium in high-risk patients with diabetes. We propose that an infusion of amino acids prior to the administration of contrast dye, will increase renal plasma flow and glomerular filtration rate by approximately 20% and hasten excretion of the contrast agent thereby protecting high-risk patients from contrast nephropathy. This is a double-blind, randomized, placebo-controlled trial evaluating the effectiveness of an amino-acid infusion in addition to usual therapy (intravenous normal saline infusion) for the prevention of renal dysfunction following angiographic dye administration during coronary angiography in a high risk group of patients with chronic renal insufficiency. Comparison: Primary and secondary outcomes in patients receiving intravenous amino acid infusion compared to placebo group receiving intravenous normal saline.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Contrast Nephropathy, Renal Failure
    Keywords
    contrast nephropathy, renal failure, Travasol

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare Provider
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Active Comparator
    Arm Description
    Intravenous saline infusion plus amino acid infusion
    Arm Title
    2
    Arm Type
    Placebo Comparator
    Arm Description
    Intravenous saline infusion plus placebo infusion
    Intervention Type
    Drug
    Intervention Name(s)
    Amino Acid
    Other Intervention Name(s)
    Parenteral nutrition
    Intervention Description
    7% amino acid infusion
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Other Intervention Name(s)
    Normal Saline Infusion
    Intervention Description
    0.9% Saline Infusion
    Primary Outcome Measure Information:
    Title
    to assess if the infusion of amino acids will help prevent kidney damage that can occur when angiographic dye is used to perform a cardiac catheterization
    Time Frame
    Day 0 to Day 7
    Secondary Outcome Measure Information:
    Title
    the serum cystatin C level at 24 hours post procedure and 72 hours post procedure
    Time Frame
    Day 0 to Day 3
    Title
    the number of patients with a peak increase in serum creatinine concentration of at least 44.1 umol/L between day 0 and day 3 (72 hours)
    Time Frame
    Day 0 to Day 3
    Title
    the number of patients with a peak increase in serum creatinine concentration of at least 88.4 μmol per liter between day 0 and day 3 (72 hours) post-catheterization
    Time Frame
    Day 0 to Day 3
    Title
    development of heart failure or myocardial infarction within 7 days
    Time Frame
    7 days
    Title
    need for renal replacement therapy
    Time Frame
    7days
    Title
    death at 48 hours, 7 days, or 14 days post-catheterization
    Time Frame
    14 days
    Title
    number of hospital days after catheterization
    Time Frame
    7 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Greater then 18 years of age Referral for coronary angiography Type 1 or type 2 diabetic requiring insulin or oral hypoglycemic agents Stable serum creatinine concentration (140 to 300 μmol per liter for men or 125 to 300 μmol per liter for women or a creatinine clearance not greater than 60 ml/min (as calculated by Cockcroft-Gault equation) Non diabetic subjects with a stable serum creatinine concentration of 160 to 300 µmol per liter for men and 140 to 300 µmol per liter for women. Stable renal function defined as no documented rise or fall in serum creatinine by more then 44 umol/L in the preceding 2 weeks Exclusion Criteria: Refusal or inability to give consent Pregnant Non-elective coronary angiography Recent administration (within 21 days) of iodinated intravenous contrast dye Recent administration (within 21 days) of non-steroidal anti-inflammatory drugs (excluding aspirin), aminoglycoside antibiotics or chemotherapeutic agents Severe/unstable diabetics requiring emergency room or inpatient therapy in the previous 21 days Compensated or decompensated hepatic failure Renal transplant
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Karen E Yeates, MD MPH
    Organizational Affiliation
    Assistant Professor, Queen's University - Division of Nephrology, Department of Medicine
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Study of Intravenous Amino Acid Infusion to Prevent Contrast Dye Mediated Renal Damage

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