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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06349577
Other study ID # 23-0921
Secondary ID 5K23HL151882
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 2024
Est. completion date October 2028

Study information

Verified date April 2024
Source University of Colorado, Denver
Contact Nathan J Clendenen, MD,MS
Phone 3037245000
Email nathan.clendenen@cuanschutz.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective is to determine the effectiveness of pulsatile flow during cardiopulmonary bypass to reduce the incidence of acute kidney injury after cardiac surgery. Investigators will also evaluate the safety and impact of pulsatile flow on clinical outcomes compared to non-pulsatile flow during cardiopulmonary bypass.


Description:

Non-pulsatile and pulsatile blood flow during cardiopulmonary bypass for cardiac surgery are both considered standard of care and allow surgeons to operate on the heart without movement. Pulsatile cardiopulmonary bypass produces variations in blood flow to produce a pulse similar to a normal beating heart. Non-pulsatile and pulsatile blood flow during cardiopulmonary bypass are approved as safe and effective ways to provide perfusion during cardiac surgery, but it is unknown whether there are differences in clinical outcomes after surgery. Acute kidney injury is common after cardiac surgery and may be caused by inadequate perfusion during cardiopulmonary bypass. Specific Aim: The purpose of this study is to determine the effectiveness of pulsatile blood flow during cardiopulmonary bypass to reduce the incidence of acute kidney injury after cardiac surgery compared to non-pulsatile blood flow. Hypothesis: Pulsatile blood flow during cardiopulmonary bypass will reduce the incidence of acute kidney injury after cardiac surgery compared to non-pulsatile blood flow.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1100
Est. completion date October 2028
Est. primary completion date April 2028
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Able to provide informed consent - Scheduled for elective cardiac surgery with cardiopulmonary bypass Exclusion Criteria - Emergency procedures - Scheduled for heart or lung transplantation - Scheduled for ventricular assist device implantation - Use of the Medtronic Elongated Once-Piece Arterial Cannula - Diagnosed with sepsis - Diagnosed with delirium - Experiencing hemodynamic instability (heart rate > 100 and systolic blood pressure < 90) - Requiring mechanical circulatory support - Requiring vasoactive medications

Study Design


Intervention

Other:
Non-pulsatile blood flow
Non-pulsatile blood flow generated by constant centrifugal pump flow rate during cardiopulmonary bypass
Pulsatile blood flow
Pulsatile blood flow generated by variable centrifugal pump flow rate during cardiopulmonary bypass

Locations

Country Name City State
United States University of Colorado Hospital Aurora Colorado

Sponsors (2)

Lead Sponsor Collaborator
University of Colorado, Denver National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

References & Publications (3)

Demirjian S, Bashour CA, Shaw A, Schold JD, Simon J, Anthony D, Soltesz E, Gadegbeku CA. Predictive Accuracy of a Perioperative Laboratory Test-Based Prediction Model for Moderate to Severe Acute Kidney Injury After Cardiac Surgery. JAMA. 2022 Mar 8;327(10):956-964. doi: 10.1001/jama.2022.1751. — View Citation

Khwaja A. KDIGO clinical practice guidelines for acute kidney injury. Nephron Clin Pract. 2012;120(4):c179-84. doi: 10.1159/000339789. Epub 2012 Aug 7. No abstract available. — View Citation

Tan A, Newey C, Falter F. Pulsatile Perfusion during Cardiopulmonary Bypass: A Literature Review. J Extra Corpor Technol. 2022 Mar;54(1):50-60. doi: 10.1182/ject-50-60. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Myocardial infarction Myocardial infarction by clinical diagnosis From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Stroke Stroke by clinical diagnosis From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Renal failure requiring renal replacement therapy New diagnosis of renal failure requiring renal replacement therapy From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Re-exploration for bleeding Surgical re-exploration for bleeding From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Sepsis Diagnosed by positive blood culture From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other New onset atrial fibrillation Clinical diagnosis of new onset atrial fibrillation From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Duration of mechanical ventilation Duration of mechanical ventilation From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Post-operative delirium Post-operative determined by the Confusion Assessment Method for the Intensive Care Unit From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Post-operative hospital length of stay Post-operative hospital length of stay From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other New requirement for mechanical circulatory support New requirement for mechanical circulatory support From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Intra-operative red blood cell transfusion in units Intra-operative red blood cell transfusion in units During the intra-operative time period, up to 12 hours
Other Post-operative red blood cell transfusion in units Post-operative red blood cell transfusion in units From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Post-operative platelet transfusion in units Post-operative platelet transfusion in units From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Post-operative plasma transfusion in units Post-operative plasma transfusion in units From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Post-operative cryoprecipitate transfusion in units Post-operative cryoprecipitate transfusion in units From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other Intra-operative platelet transfusion in units Intra-operative platelet transfusion in units During the intra-operative time period, up to 12 hours
Other Intra-operative plasma transfusion in units Intra-operative plasma transfusion in units During the intra-operative time period, up to 12 hours
Other Intra-operative cryoprecipitate transfusion in units Intra-operative cryoprecipitate transfusion in units During the intra-operative time period, up to 12 hours
Other New onset of acute lung injury Diagnosis of acute lung injury by PaO2 to FiO2 ratio = 300 From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other New onset of left ventricular systolic dysfunction New onset of left ventricular systolic dysfunction determined by a LV ejection fraction <50% From intensive care unit admission after surgery to hospital discharge, up to 30 days
Other New onset of right ventricular systolic dysfunction New onset of right ventricular systolic dysfunction determined by a tricuspid annular plane systolic excursion less than 16 mm From intensive care unit admission after surgery to hospital discharge, up to 30 days
Primary Acute kidney injury Stage 1 (mild), 2 (moderate), or 3 (severe) acute kidney injury according to the Kidney Disease Improving Global Outcomes creatinine criteria (stage 1 = 1.5 to 1.9 times baseline or greater than or equal to 0.3 milligrams per deciliter increase in serum creatinine, stage 2 = 2.0 to 2.9 times baseline in serum creatinine, stage 3 = 3.0 times baseline or increase in serum creatinine greater than or equal to 4.0 milligrams per deciliter or initiation of renal replacement therapy From intensive care unit admission after surgery up to 7 days
Secondary Acute kidney injury risk score Demirjian Perioperative Laboratory Test-Based Prediction Model for Moderate to Severe Acute Kidney Injury After Cardiac Surgery in percent predicted risk On admission to the intensive care unit after surgery up to 24 hours after intensive care unit arrival
Secondary Red blood cell units transfused Number of allogenic red blood cell units transfused after cardiopulmonary bypass After cardiopulmonary bypass up to 24 hours after intensive care unit arrival
Secondary Platelet nadir Lowest platelet count after cardiopulmonary bypass On admission to the intensive care unit after surgery up to 7 days
Secondary Discontinuation rate of cardiopulmonary bypass mode Discontinuation rate of pulsatile or non-pulsatile cardiopulmonary bypass mode During cardiopulmonary bypass
Secondary 30-day mortality All cause mortality From intensive care unit admission after surgery to hospital discharge, up to 30 days
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