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Veno-venous Extracorporeal Membrane Oxygenation (VV-ECMO) Heparin Study

Single Center Open Label Randomized Study Evaluating Safety and Efficacy of Subcutaneous Heparin Compared to Standard of Care Intravenous Heparin Anticoagulation During Veno-venous Extracorporeal Membrane Oxygenation for Respiratory Failure

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04496362
Enrollment
100
Registered
2020-08-03
Start date
2018-10-10
Completion date
2026-06-01
Last updated
2026-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ECMO, Heparin, Respiratory Failure

Brief summary

This single-center, open-label study will evaluate the safety and efficacy of subcutaneous heparin anticoagulation compared to the standard of care systemic intravenous anticoagulation during veno-venous extracorporeal membrane oxygenation for respiratory failure.

Detailed description

Extracorporeal membrane oxygenation (ECMO) has been increasing used over the past decade as supportive therapy in patients with respiratory failure, in order to avoid life-threatening hypoxemia, in cases otherwise refractory to conventional treatment. Veno-venous ECMO (VV ECMO) removes carbon dioxide and significantly improves oxygenation in patients with severe lung failure. System anticoagulation is provided for patients undergoing ECMO therapy to prevent clot formation in the ECMO circuit cannulas, circuit tubing, centrifugal pump, and/or oxygenator. Heparin is the standard anticoagulant for ECMO therapy. Although technological advancements and increasing clinical experience have made the use of VV ECMO safer, bleeding and thrombosis are common complications accounting for the majority of morbidity and mortality in ECMO-treated patients.The optimal anticoagulation management for patients on VV ECMO is not known. Thrombotic episodes, characterized mainly by circuit-related clotting, have become more manageable with improvements in ECMO circuit technology and heparin-coated lines. The Extracorporeal Life Support Organization (ELSO) guidelines describe bleeding as the most common complication during extracorporeal life support. Bleeding has been reported to occur in as many as 30% of patients receiving ECMO therapy, and depending on the site of the hemorrhagic complication, can be fatal. Bleeding may occur from mucous membranes, the uterus in women in childbearing years, the GI tract, or bleeding into the head or brain parenchyma. Intra-cranial hemorrhage is the most serious and usually extensive and fatal complication.Intra-cranial hemorrhage was identified in more than 40% of non-survivors treated with ECMO during the H1N1 flu outbreak of 2009. Other less serious complications associated with anticoagulation are anemia and the risks associated with transfusions. Review of our own institutional ECMO experience revealed 10 cases of VV ECMO during which anticoagulation had to be held for clinical reasons, all without subsequent increases in thrombotic complications. Identifying the safest approach to anticoagulation is essential to the future management of patients on ECMO support. In this prospective randomized clinical trial, the investigators propose to evaluate the safety and efficacy of subcutaneous heparin anticoagulation compared to the standard of care systemic intravenous anticoagulation in subjects requiring veno-venous extracorporeal membrane oxygenation for respiratory failure.

Interventions

DRUGsubcutaneous heparin anticoagulation

The primary objective of this study is to evaluate the safety and efficacy of subcutaneous heparin anticoagulation compared to the standard of care systemic intravenous anticoagulation during veno-venous extracorporeal membrane oxygenation for respiratory failure. Subjects will be prospectively randomized in 1:1 ratio to subcutaneous heparin anticoagulation or systemic intravenous anticoagulation and followed until 1 week after discontinuation from ECMO support.

Sponsors

Baylor Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female ≥ 18 years of age 2. Respiratory failure requiring VV-ECMO support 3. Subject or appointed health care proxy/LAR is able to understand and sign the informed consent form

Exclusion criteria

1. Subject currently enrolled in another interventional research trial 2. History of hypersensitivity/adverse reaction to heparin 3. Proven Heparin induced thrombocytopenia (HIT) 4. History of patent foramen ovale (PFO) 5. Recent surgery or other contraindication to systemic anticoagulation, e.g. intracranial bleed 6. Medical indication other than ECMO for systemic anticoagulation, e.g. pulmonary embolism

Design outcomes

Primary

MeasureTime frameDescription
Incidence of bleeding complication1 weekSafety will be assessed by incidence of bleeding complication (clinically apparent or need for blood transfusion without identified source)
Incidence of thrombotic complications requiring intervention1 weekSafety will be assessed by incidence of thrombotic complications requiring intervention (initiation of systemic anticoagulation or oxygenator exchange)
Incidence of deep venous thrombosis1 weekIncidence of deep venous thrombosis as assessed by four extremity venous ultrasound at one week post-decannulation

Secondary

MeasureTime frameDescription
Mortality1 yearDirectly related to bleeding and clotting

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORGary Schwartz, MD

BSWH

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026