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NAD+ Augmentation in Cardiac Surgery Associated Myocardial Injury Trial

NAD+ Augmentation in Cardiac Surgery Associated Myocardial Injury Trial

Recruiting
18 years and older
All
Phase 2

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Overview

A Randomized, Double-blind, placebo-controlled Trial to Evaluate the Efficacy of Oral Nam for the Prevention of Acute Kidney Injury in Patients Undergoing On-Pump Cardiac Surgery

Description

This trial is a single-center, randomized, double-blind placebo-controlled Trial of Nam versus placebo in patients undergoing on-pump cardiac surgery. After screening and enrollment, patients will be stratified according to CKD status (eGFR<45 ml/min/m2) and surgical site and randomized in a 1:1 manner to receive either Nam 3 grams or placebo on the day of surgery and post-surgical days one and two.

The overall trial duration is planned for 42 months, consisting of 39 months of active recruitment and treatment period and three months of follow-up from the last patient enrolled.

Eligibility

Inclusion Criteria

  • Informed consent before any study-related activities.
  • Men or women >18 years of age who are scheduled for non-emergent cardiac surgery procedures requiring CPB and are at increased risk for surgery-related adverse cardiovascular outcomes.

Procedures include:

  • CABG
  • Aortic, mitral, tricuspid, or pulmonic valve replacement or repair
  • CABG with aortic, mitral, tricuspid, and/or pulmonic valve replacement
        Risk factors for surgery related to adverse cardiovascular outcomes include one or more of
        the following:
          -  Valve surgery
          -  eGFR < 45 ml/min/1.73m2
          -  Documented LVEF ≤ 35% within six months before surgery
          -  Documented history of heart failure
          -  Insulin-requiring diabetes
          -  Non-insulin-requiring diabetes and the presence of ≥+2 proteinuria on urinalysis (or
             equivalent on urine protein-to-creatinine ratio or urine albumin-to-creatinine ratio)
          -  Preoperative anemia (hemoglobin <11g/dl for men and women)
          -  History of prior CABG
          -  Age ≥65
        Exclusion Criteria
          -  Preexisting AKI within seven days before surgery as defined by KDIGO stage ≥1 (serum
             creatinine-based)
          -  Kidney transplant status
          -  Off-pump cardiac surgery
          -  ESRD
          -  Emergent cardiac surgery
          -  Pregnancy
          -  Patient enrolled in competing research studies that may affect outcomes
          -  Patients held in an institution by legal or official order

Study details
    Ischemia Reperfusion Injury
    Myocardial Injury
    Acute Kidney Injury

NCT04750616

Kaiser Permanente

26 January 2024

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