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Study Using Citrate to Replace Heparin in Babies Requiring Extracorporeal Membrane Oxygenation (ECMO)

Primary Purpose

Heart Defects, Congenital, Respiratory Insufficiency

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
sodium citrate
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Defects, Congenital focused on measuring Heart Defects, Congenital, Extracorporeal Membrane Oxygenation, Citric Acid, Heparin, Respiratory Insufficiency

Eligibility Criteria

1 Day - 1 Year (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infant less than one year of age and less than 6 kg
  • Informed consent obtained from parent
  • One or more of the following diagnoses:
  • Post-op congenital heart surgery
  • Congenital diaphragmatic hernia
  • Sepsis with coagulopathy not corrected prior to ECMO
  • Other newborn diagnosis with Grade I or II IVH
  • Infant requires/is on ECMO

Exclusion Criteria:

  • Consent denied or unobtainable
  • Age greater than one year
  • Weight greater than 6 kg
  • Gestational age less than 34 weeks

Sites / Locations

  • Vanderbilt Children's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Citrate

Arm Description

Sodium citrate will be infused as the blood enters the ECMO circuit and calcium chloride will be infused as the blood leaves the ECMO circuit and enters the patient

Outcomes

Primary Outcome Measures

anticoagulation of ECMO circuit while maintaining normal coagulation and calcium levels in patient

Secondary Outcome Measures

Maintain normal serum calcium levels in patients

Full Information

First Posted
August 28, 2009
Last Updated
June 1, 2015
Sponsor
Vanderbilt University
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1. Study Identification

Unique Protocol Identification Number
NCT00968565
Brief Title
Study Using Citrate to Replace Heparin in Babies Requiring Extracorporeal Membrane Oxygenation (ECMO)
Official Title
Regional Citrate Anticoagulation in ECMO
Study Type
Interventional

2. Study Status

Record Verification Date
June 2010
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine the safety and efficacy of citrate to provide anticoagulation of an ECMO circuit without patient anticoagulation. The standard method of providing ECMO circuit anticoagulation is the use of heparin which also anticoagulates the patient and increases the risk of patient bleeding.
Detailed Description
Extracorporeal membrane oxygenation (ECMO) is a form of extended heart/lung bypass support that has been used to treat more than 650 patients over 20 years at Vanderbilt. Over 29,000 patients have been treated worldwide. Bleeding is the most common complication during ECMO because of systemic anticoagulation with heparin. It is most commonly seen in patients following surgery either preceding or while on ECMO support. Regional citrate anticoagulation for hemodialysis was first introduced in 1961. It is the ideal alternative to heparin in patients who are at increased risk for bleeding. It permits effective anticoagulation across the extracorporeal circuit without impacting the patient's systemic coagulation. Citrate functions by binding free calcium, thereby inhibiting coagulation in both the intrinsic and extrinsic coagulation pathways. The purpose of this study is to evaluate the use of citrate as a regional anticoagulant in the ECMO circuit in high risk infants less than one year of age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Defects, Congenital, Respiratory Insufficiency
Keywords
Heart Defects, Congenital, Extracorporeal Membrane Oxygenation, Citric Acid, Heparin, Respiratory Insufficiency

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Citrate
Arm Type
Experimental
Arm Description
Sodium citrate will be infused as the blood enters the ECMO circuit and calcium chloride will be infused as the blood leaves the ECMO circuit and enters the patient
Intervention Type
Drug
Intervention Name(s)
sodium citrate
Intervention Description
Continuous infusion of 4% sodium citrate at 300 ml/hour into ECMO circuit
Primary Outcome Measure Information:
Title
anticoagulation of ECMO circuit while maintaining normal coagulation and calcium levels in patient
Time Frame
hourly
Secondary Outcome Measure Information:
Title
Maintain normal serum calcium levels in patients
Time Frame
hourly

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infant less than one year of age and less than 6 kg Informed consent obtained from parent One or more of the following diagnoses: Post-op congenital heart surgery Congenital diaphragmatic hernia Sepsis with coagulopathy not corrected prior to ECMO Other newborn diagnosis with Grade I or II IVH Infant requires/is on ECMO Exclusion Criteria: Consent denied or unobtainable Age greater than one year Weight greater than 6 kg Gestational age less than 34 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John B Pietsch, MD
Organizational Affiliation
Vanderbilt University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt Children's Hospital
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
6848936
Citation
Pinnick RV, Wiegmann TB, Diederich DA. Regional citrate anticoagulation for hemodialysis in the patient at high risk for bleeding. N Engl J Med. 1983 Feb 3;308(5):258-61. doi: 10.1056/NEJM198302033080506. No abstract available.
Results Reference
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PubMed Identifier
16139156
Citation
Bagshaw SM, Laupland KB, Boiteau PJ, Godinez-Luna T. Is regional citrate superior to systemic heparin anticoagulation for continuous renal replacement therapy? A prospective observational study in an adult regional critical care system. J Crit Care. 2005 Jun;20(2):155-61. doi: 10.1016/j.jcrc.2005.01.001.
Results Reference
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PubMed Identifier
19092671
Citation
Suzuki Y, Yamauchi S, Daitoku K, Fukui K, Fukuda I. Extracorporeal membrane oxygenation circulatory support after congenital cardiac surgery. ASAIO J. 2009 Jan-Feb;55(1):53-7. doi: 10.1097/MAT.0b013e31818f0056.
Results Reference
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PubMed Identifier
18272829
Citation
Clark JA, Schulman G, Golper TA. Safety and efficacy of regional citrate anticoagulation during 8-hour sustained low-efficiency dialysis. Clin J Am Soc Nephrol. 2008 May;3(3):736-42. doi: 10.2215/CJN.03460807. Epub 2008 Feb 13.
Results Reference
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Study Using Citrate to Replace Heparin in Babies Requiring Extracorporeal Membrane Oxygenation (ECMO)

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