This study seeks to compare outcomes of 2 different methods of cardiopulmonary support during
lung transplant surgeries.
Device: Extracorporeal Membrane Oxygenation
Device: Cardiopulmonary Bypass
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Locations near you
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Full eligibility criteria for NCT03021538
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
The study population will be all patients requiring cardiopulmonary support while undergoing lung transplantation at our institution.
Patients undergoing concomitant cardiac operations with indication for obligate use of cardiopulmonary bypass
Patient with specific anatomy that require full cardiac decompression such as severe pulmonary hypertension or large heart that are shifted severely into the left chest
Patients with high likelihood of significant pleural bleeding that will require returning the blood back into the cardiotomy reservoir
Patients bridged to transplant with ECMO
Cystic fibrosis/bronchiectasis/resistant infection patients where surgeon will need to remove both lungs prior to implantation
Patients who the surgeon feels would be better served with CPB rather than ECMO- These patients will be entered into a registry and followed.
All locations for NCT03021538
United States (1)
Cleveland, Ohio, United States, 44195
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View full eligibility
Tris trial is registered with FDA with number: NCT03021538. The sponsor of the trial is The Cleveland Clinic and it is looking for 80 volunteers for the current phase.
Official trial title: Randomized Clinical Trial of Intraoperative Extracorporeal Membrane Oxygenation (ECMO) Versus Cardiopulmonary Bypass (CPB) in Lung Transplantation
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