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High-exchange ULTrafiltration to Enhance Recovery After Pediatric Cardiac Surgery (ULTRA)

Primary Purpose

Congenital Heart Disease

Status
Recruiting
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Ultrafiltration
Sponsored by
IWK Health Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congenital Heart Disease

Eligibility Criteria

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

Inclusion Criteria:

  • Congenital heart patients (2.5 - 15kg) have consented for a planned cardiac surgery procedure requiring cardiopulmonary bypass.
  • Parent or legal substitute decision-maker informed written consent to participate in the study.

Exclusion Criteria:

  • Patient or family refusal to participate.
  • Patient over 15kg (Fontan or Glenn patients will be considered up to 18kg)
  • No planned use of cardiopulmonary bypass
  • Isolated ASD repair
  • Known severe hematologic abnormality such as sick cell anemia, thalassemia, haemophilia A or B, von Willebrand disease or other.
  • Known genetic syndrome with severe neurologic or multi-organ abnormalities and immune dysfunction such as DiGeorge Syndrome, Trisomy 18 or 13, Noonan syndrome. (Trisomy 21 may be included in the study).
  • Known immunodeficiency syndrome or bone marrow pathology.
  • Severe liver or renal disease.

Sites / Locations

  • IWK Health CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

High-Exchange Ultrafiltration

Low-Exchange Ultrafiltraiton

Arm Description

Subzero-Balance Simple Modified Ultrafiltration (60ml/kg/hour)

Subzero-Balance Simple Modified Ultrafiltration (6ml/kg/hour)

Outcomes

Primary Outcome Measures

Peak Vasoactive-Ventilation Renal Score

Secondary Outcome Measures

Vasoactive Inotrope Score
Ventilation Index
Oxygenation Index
Ventilation Time
Ventilator Free Days
Low Cardiac Output Syndrome
Pre-specified criteria
Vasoplegic Shock
Pre-specified criteria
Inotrope Dependence
Pre-specified criteria
Inotrope Free Days
C-Reactive Protein Concentrations
Composite Outcome of mechanical circulatory support, acute renal failure, prolonged intubation and death within 30 days.
Pre-specified criteria
Cytokine Concentration
Plasma concentrations measured by Luminex. (specific cytokines to be selected based on Pilot study results)

Full Information

First Posted
May 30, 2021
Last Updated
December 24, 2022
Sponsor
IWK Health Centre
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1. Study Identification

Unique Protocol Identification Number
NCT04920643
Brief Title
High-exchange ULTrafiltration to Enhance Recovery After Pediatric Cardiac Surgery
Acronym
ULTRA
Official Title
High-exchange ULTrafiltration to Enhance Recovery After Pediatric Cardiac Surgery (ULTRA): A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 28, 2021 (Actual)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
June 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IWK Health Centre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Malformations of the heart are common; 1.35 million infants are born each year with congenital heart disease. Many of these defects carry a considerable threat to the individual's quality of life as well as survival. Along with focused medical management, surgical repair remains a standard of care for more than 25,000 infants and children each year in the United States and Canada. The care of individuals with congenital heart disease is highly complex and has significant risks of morbidity and mortality. Most cardiac operations require the use of cardiopulmonary bypass (CPB, also known as the heart-lung machine) to safely access the inner chambers of the heart. CPB itself has been well documented to cause significant inflammation and hemodilution as the individual's blood is passed through a foreign circuit. This inflammatory response can lead to fluid overload, distributive shock and potential end-organ dysfunction in the heart, lungs, kidneys, brain, liver or bowels. These organ dysfunctions may culminate in post-operative low cardiac output syndrome (LCOS), prolonged ventilation time, prolonged intensive care unit (ICU) stay and can contribute to mortality. Dampening the inflammatory response from CPB has been a focus of research interest for years. Intra-operative ultrafiltration has been used to remove excess fluids and filter off inflammatory cytokines during cardiac operations. Over 90% of children's heart centers in the world utilize some form of ultrafiltration (mostly some form of modified ultrafiltration), but there are wide variations in published ultrafiltration protocols (none of which are combination SBUF-SMUF in children). Ultimately, this project seeks to provide high-quality evidence that the immunologic and clinical effects of combination SBUF-SMUF are rate dependent. Therefore, a randomized study directly comparing a high-exchange SBUF-SMUF (60ml/kg/hr) and a low-exchange SBUF-SMUF (6ml/kg/hr) can identify which is the optimal ultrafiltration protocol to enhance post-operative clinical outcomes for this patient population. The expected data and results could be immediately applicable to improve recovery after heart surgery for infants and children across Canada and the rest of the world at large.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
High-Exchange Ultrafiltration
Arm Type
Experimental
Arm Description
Subzero-Balance Simple Modified Ultrafiltration (60ml/kg/hour)
Arm Title
Low-Exchange Ultrafiltraiton
Arm Type
Active Comparator
Arm Description
Subzero-Balance Simple Modified Ultrafiltration (6ml/kg/hour)
Intervention Type
Procedure
Intervention Name(s)
Ultrafiltration
Intervention Description
Ultrafiltration is used during cardiac surgery with cardiopulmonary bypass to remove both fluid and small molecules such as inflammatory cytokines from the patient's circulation.
Primary Outcome Measure Information:
Title
Peak Vasoactive-Ventilation Renal Score
Time Frame
Up to 5 days
Secondary Outcome Measure Information:
Title
Vasoactive Inotrope Score
Time Frame
Up to 5 days
Title
Ventilation Index
Time Frame
Up to 5 days
Title
Oxygenation Index
Time Frame
Up to 5 days
Title
Ventilation Time
Time Frame
Up to 30 days
Title
Ventilator Free Days
Time Frame
Up to 30 days
Title
Low Cardiac Output Syndrome
Description
Pre-specified criteria
Time Frame
Up to 3 days
Title
Vasoplegic Shock
Description
Pre-specified criteria
Time Frame
Up to 3 days
Title
Inotrope Dependence
Description
Pre-specified criteria
Time Frame
Up to 2 days
Title
Inotrope Free Days
Time Frame
Up to 30 days
Title
C-Reactive Protein Concentrations
Time Frame
Measured at 1 day
Title
Composite Outcome of mechanical circulatory support, acute renal failure, prolonged intubation and death within 30 days.
Description
Pre-specified criteria
Time Frame
Up to 30 days
Title
Cytokine Concentration
Description
Plasma concentrations measured by Luminex. (specific cytokines to be selected based on Pilot study results)
Time Frame
Up to 1 day

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Congenital heart patients (2.5 - 15kg) have consented for a planned cardiac surgery procedure requiring cardiopulmonary bypass. Parent or legal substitute decision-maker informed written consent to participate in the study. Exclusion Criteria: Patient or family refusal to participate. Patient over 15kg (Fontan or Glenn patients will be considered up to 18kg) No planned use of cardiopulmonary bypass Isolated ASD repair Known severe hematologic abnormality such as sick cell anemia, thalassemia, haemophilia A or B, von Willebrand disease or other. Known genetic syndrome with severe neurologic or multi-organ abnormalities and immune dysfunction such as DiGeorge Syndrome, Trisomy 18 or 13, Noonan syndrome. (Trisomy 21 may be included in the study). Known immunodeficiency syndrome or bone marrow pathology. Severe liver or renal disease.
Facility Information:
Facility Name
IWK Health Centre
City
Halifax
State/Province
Nova Scotia
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joel Bierer, MD
Phone
519-819-8439
Email
joelbierer@gmail.com
First Name & Middle Initial & Last Name & Degree
David Horne, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31701831
Citation
Bierer J, Stanzel R, Henderson M, Sett S, Horne D. Ultrafiltration in Pediatric Cardiac Surgery Review. World J Pediatr Congenit Heart Surg. 2019 Nov;10(6):778-788. doi: 10.1177/2150135119870176.
Results Reference
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High-exchange ULTrafiltration to Enhance Recovery After Pediatric Cardiac Surgery

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