Fixed Low-dose Heparin Versus Standard Adjusted-dose Heparin Infusion in Adults Receiving Venovenous ECMO With a Heparin Bonded Circuit.
Primary Purpose
Acute Respiratory Failure, Extracorporeal Membrane Oxygenation Complication, Bleeding
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
HEP-IV
Sponsored by
About this trial
This is an interventional supportive care trial for Acute Respiratory Failure focused on measuring extracorporeal membrane oxygenation, intravenous heparin
Eligibility Criteria
Inclusion Criteria:
- on ECMO for acute respiratory failure, achieving ECMO blood flow rate >3L/min,
- patient or surrogate able to speak/understand English or Spanish
Exclusion Criteria:
- History of heparin-induced thrombocytopenia, decision by clinicians to run ECMO off heparin due to high bleeding risk,
- pregnancy
Sites / Locations
- Banner - University Medical Center Phoenix
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Adjusted-dose heparin
Fixed low-dose heparin
Arm Description
Patients in this arm of the study will receive intravenous unfractionated heparin at a dose adjusted to achieve an activated clotting time of 180-200 seconds.
Patients in this arm of the study will receive intravenous unfractionated heparin at 500 units/hour without activated clotting time monitoring.
Outcomes
Primary Outcome Measures
significant bleeding complications
requires surgery, >1 unit packed blood cell transfusion or is intracranial, pulmonary or retroperitoneal
Secondary Outcome Measures
Oxygenator failure
Requirement to replace oxygenator due to clotting
cerebral vascular event (stroke)
Full Information
NCT ID
NCT02966080
First Posted
November 15, 2016
Last Updated
August 16, 2017
Sponsor
University of Arizona
1. Study Identification
Unique Protocol Identification Number
NCT02966080
Brief Title
Fixed Low-dose Heparin Versus Standard Adjusted-dose Heparin Infusion in Adults Receiving Venovenous ECMO With a Heparin Bonded Circuit.
Official Title
Fixed Low-dose Heparin Versus Standard Adjusted-dose Heparin Infusion in Adults Receiving Venovenous Extracorporeal Membrane Oxygenation (ECMO) With a Heparin Bonded Circuit.
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Withdrawn
Why Stopped
No participants enrolled, study will not be conducted.
Study Start Date
December 2016 (undefined)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
February 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Arizona
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Heparin is a blood thinner used to prevent blood clots in patients on a form of life-support called ECMO. Heparin can cause bleeding - the most common complication of ECMO. New materials used in ECMO machines may help prevent clots - this could allow the use of lower doses of heparin which might reduce the risk of bleeding. Our study will compare low dose to high dose heparin in patients on ECMO. We think low dose heparin may be adequate to prevent clotting, but may cause less bleeding and be safer for patients.
Detailed Description
Intravenous heparin is considered standard therapy to prevent clotting complications in patients on ECMO, however the optimal method of heparin dosing has not yet been determined. International surveys have shown that most ECMO centers use adjusted dose heparin to achieve an activated clotting time of at least 180 seconds. However, heparin may contribute to the most common complication of ECMO - bleeding. Advances in material technology have potentially reduced the thrombogenicity of modern ECMO circuits. Our observational data suggest that fixed low dose heparin infusion may reduce the rate of bleeding complications from 75% to 50% compared to standard adjusted-dose heparin, without increasing clotting complications. We intend to perform a randomized controlled trial in adults receiving venovenous ECMO comparing these two heparin regimens. The main outcome measures are bleeding complications and oxygenator failure due to clotting. A safety committee will monitor the results of the study. Power calculations indicate a sample size of 110 patients is required, which we estimate will take us five years to achieve.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Failure, Extracorporeal Membrane Oxygenation Complication, Bleeding
Keywords
extracorporeal membrane oxygenation, intravenous heparin
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Adjusted-dose heparin
Arm Type
Other
Arm Description
Patients in this arm of the study will receive intravenous unfractionated heparin at a dose adjusted to achieve an activated clotting time of 180-200 seconds.
Arm Title
Fixed low-dose heparin
Arm Type
Other
Arm Description
Patients in this arm of the study will receive intravenous unfractionated heparin at 500 units/hour without activated clotting time monitoring.
Intervention Type
Drug
Intervention Name(s)
HEP-IV
Other Intervention Name(s)
heparin
Primary Outcome Measure Information:
Title
significant bleeding complications
Description
requires surgery, >1 unit packed blood cell transfusion or is intracranial, pulmonary or retroperitoneal
Time Frame
intraoperative
Secondary Outcome Measure Information:
Title
Oxygenator failure
Description
Requirement to replace oxygenator due to clotting
Time Frame
intraoperative
Title
cerebral vascular event (stroke)
Time Frame
intraoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
on ECMO for acute respiratory failure, achieving ECMO blood flow rate >3L/min,
patient or surrogate able to speak/understand English or Spanish
Exclusion Criteria:
History of heparin-induced thrombocytopenia, decision by clinicians to run ECMO off heparin due to high bleeding risk,
pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Raschke, MD
Organizational Affiliation
Banner University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Banner - University Medical Center Phoenix
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85006
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
24651227
Citation
Esper SA, Levy JH, Waters JH, Welsby IJ. Extracorporeal membrane oxygenation in the adult: a review of anticoagulation monitoring and transfusion. Anesth Analg. 2014 Apr;118(4):731-43. doi: 10.1213/ANE.0000000000000115.
Results Reference
background
Citation
Poulos EM, Raschke R, Amabile O et al. A Nonrandomized comparison of three different heparin infusion strategies for patients receiving venovenous extracorporeal membrane oxygenation. Am J Respir Crit Care Med 2014;189: A4499.
Results Reference
background
Links:
URL
http://www.elso.org
Description
ELSO anticoagulation guideline
Learn more about this trial
Fixed Low-dose Heparin Versus Standard Adjusted-dose Heparin Infusion in Adults Receiving Venovenous ECMO With a Heparin Bonded Circuit.
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