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CTI-01 (Ethyl Pyruvate) Safety and Complication Prevention in Cardiac Surgery Patients on Cardiopulmonary Bypass (CPB)

Primary Purpose

Coronary Disease, Heart Valve Diseases

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
CTI-01 (ethyl pyruvate)
Sponsored by
Critical Therapeutics
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Coronary Disease focused on measuring Coronary artery bypass grafting, Heart valve prosthesis implantation, Cardiopulmonary bypass, Oxidative stress, Inflammation, Endotoxemia

Eligibility Criteria

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

Inclusion Criteria: Parsonnet additive risk score greater than or equal to 15 Scheduled CABG (coronary artery bypass grafting) and/or cardiac valve repair or replacement surgery using cardiopulmonary bypass Exclusion Criteria: Emergency cardiac surgery Significant concomitant surgery Minimally invasive or thoracic surgical approach Preoperative mechanical assist device Body weight <50 kg or >140 kg Active systemic infection Creatinine >3.0 mg/dL History of hematologic or coagulation disorders History of malignancy (past year)or organ transplantation Use of immunosuppressive drugs or current immunosuppressed condition

Sites / Locations

  • Saddleback Memorial Medical Center
  • University of Southern California
  • Kaiser Permanente
  • Washington Hospital Center
  • University of Florida
  • Research Support Personnel
  • Peninsula Regional Medical Center
  • Baystate Medical Center
  • Nebraska Methodist Hospital
  • NYU Medical Center
  • Duke University Medical Center
  • East Carolina University - Brody School of Medicine
  • Hospital of the University of Pennsylvania
  • Chester County Hospital - The Cardiovasular Center
  • St. Luke's Episcopal Hospital/Texas Heart Institute
  • MultiCare Health System
  • Medical College of Wisconsin - VA Medical Center

Outcomes

Primary Outcome Measures

Death
Composite morbidity endpoint

Secondary Outcome Measures

Respiratory dysfunction
Cardiac dysfunction
Renal dysfunction
Gastrointestinal dysfunction
Mental status
Length of ICU (Intensive Care Unit)/hospital stay

Full Information

First Posted
April 6, 2005
Last Updated
March 15, 2006
Sponsor
Critical Therapeutics
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1. Study Identification

Unique Protocol Identification Number
NCT00107666
Brief Title
CTI-01 (Ethyl Pyruvate) Safety and Complication Prevention in Cardiac Surgery Patients on Cardiopulmonary Bypass (CPB)
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Proof of Concept Clinical Study of CTI-01 in Patients Undergoing Major Cardiac Surgery With Cardiopulmonary Bypass
Study Type
Interventional

2. Study Status

Record Verification Date
March 2006
Overall Recruitment Status
Terminated
Study Start Date
April 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Critical Therapeutics

4. Oversight

5. Study Description

Brief Summary
Over 500,000 patients undergo cardiac surgery with CPB in the United States annually. Although mortality rates have decreased with advances in perioperative care, many patients are affected by postoperative organ dysfunction. The incidence of complications may exceed 30%. It has been speculated that an exaggerated inflammatory response to surgical trauma and the CPB machine are likely causes for this morbidity. Factors predisposing organ dysfunction include tissue injury, endotoxemia, and oxidative stress. High risk patients can be identified preoperatively through the validated Parsonnet Additive Risk Score. CTI-01 has demonstrated potent anti-inflammatory and tissue protection activity in multiple animal models of disease including pancreatitis, ischemia-reperfusion injury, sepsis, renal injury, and endotoxemia. These findings support its clinical use in critical care medicine including cardiac surgery. Patients will receive a total of six doses, administered intravenously just prior to and after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Disease, Heart Valve Diseases
Keywords
Coronary artery bypass grafting, Heart valve prosthesis implantation, Cardiopulmonary bypass, Oxidative stress, Inflammation, Endotoxemia

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
150 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
CTI-01 (ethyl pyruvate)
Primary Outcome Measure Information:
Title
Death
Title
Composite morbidity endpoint
Secondary Outcome Measure Information:
Title
Respiratory dysfunction
Title
Cardiac dysfunction
Title
Renal dysfunction
Title
Gastrointestinal dysfunction
Title
Mental status
Title
Length of ICU (Intensive Care Unit)/hospital stay

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Parsonnet additive risk score greater than or equal to 15 Scheduled CABG (coronary artery bypass grafting) and/or cardiac valve repair or replacement surgery using cardiopulmonary bypass Exclusion Criteria: Emergency cardiac surgery Significant concomitant surgery Minimally invasive or thoracic surgical approach Preoperative mechanical assist device Body weight <50 kg or >140 kg Active systemic infection Creatinine >3.0 mg/dL History of hematologic or coagulation disorders History of malignancy (past year)or organ transplantation Use of immunosuppressive drugs or current immunosuppressed condition
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Walter Newman, Ph.D.
Organizational Affiliation
Critical Therapeutics Incorporated
Official's Role
Study Director
Facility Information:
Facility Name
Saddleback Memorial Medical Center
City
Laguna Hills
State/Province
California
ZIP/Postal Code
92653
Country
United States
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Kaiser Permanente
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States
Facility Name
Washington Hospital Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States
Facility Name
Research Support Personnel
City
Wichita
State/Province
Kansas
ZIP/Postal Code
67208
Country
United States
Facility Name
Peninsula Regional Medical Center
City
Salisbury
State/Province
Maryland
ZIP/Postal Code
21801
Country
United States
Facility Name
Baystate Medical Center
City
Springfield
State/Province
Massachusetts
ZIP/Postal Code
01199
Country
United States
Facility Name
Nebraska Methodist Hospital
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68114
Country
United States
Facility Name
NYU Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
East Carolina University - Brody School of Medicine
City
Greenville
State/Province
North Carolina
ZIP/Postal Code
27834
Country
United States
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Chester County Hospital - The Cardiovasular Center
City
West Chester
State/Province
Pennsylvania
ZIP/Postal Code
19380
Country
United States
Facility Name
St. Luke's Episcopal Hospital/Texas Heart Institute
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
MultiCare Health System
City
Tacoma
State/Province
Washington
ZIP/Postal Code
98405
Country
United States
Facility Name
Medical College of Wisconsin - VA Medical Center
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53295
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
2720942
Citation
Parsonnet V, Dean D, Bernstein AD. A method of uniform stratification of risk for evaluating the results of surgery in acquired adult heart disease. Circulation. 1989 Jun;79(6 Pt 2):I3-12. Erratum In: Circulation 1990 Sep;82(3):1078.
Results Reference
background
PubMed Identifier
9039883
Citation
Bennett-Guerrero E, Ayuso L, Hamilton-Davies C, White WD, Barclay GR, Smith PK, King SA, Muhlbaier LH, Newman MF, Mythen MG. Relationship of preoperative antiendotoxin core antibodies and adverse outcomes following cardiac surgery. JAMA. 1997 Feb 26;277(8):646-50.
Results Reference
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PubMed Identifier
12209006
Citation
Ulloa L, Ochani M, Yang H, Tanovic M, Halperin D, Yang R, Czura CJ, Fink MP, Tracey KJ. Ethyl pyruvate prevents lethality in mice with established lethal sepsis and systemic inflammation. Proc Natl Acad Sci U S A. 2002 Sep 17;99(19):12351-6. doi: 10.1073/pnas.192222999. Epub 2002 Sep 3.
Results Reference
background
PubMed Identifier
15115981
Citation
Woo YJ, Taylor MD, Cohen JE, Jayasankar V, Bish LT, Burdick J, Pirolli TJ, Berry MF, Hsu V, Grand T. Ethyl pyruvate preserves cardiac function and attenuates oxidative injury after prolonged myocardial ischemia. J Thorac Cardiovasc Surg. 2004 May;127(5):1262-9. doi: 10.1016/j.jtcvs.2003.11.032.
Results Reference
background
PubMed Identifier
12544977
Citation
Fink MP. Ethyl pyruvate: a novel anti-inflammatory agent. Crit Care Med. 2003 Jan;31(1 Suppl):S51-6. doi: 10.1097/00003246-200301001-00008.
Results Reference
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CTI-01 (Ethyl Pyruvate) Safety and Complication Prevention in Cardiac Surgery Patients on Cardiopulmonary Bypass (CPB)

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