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Clinical Trials/NCT00107666
NCT00107666
Terminated
Phase 2

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

Critical Therapeutics17 sites in 1 country150 target enrollmentApril 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Coronary Disease
Sponsor
Critical Therapeutics
Enrollment
150
Locations
17
Primary Endpoint
Composite morbidity endpoint
Status
Terminated
Last Updated
20 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 2005
End Date
April 2006
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

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

Outcomes

Primary Outcomes

Composite morbidity endpoint

Death

Secondary Outcomes

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

Study Sites (17)

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