AI Cure is a research tool showing open data. Not medical advice. Discuss with your doctor. Terms

← Trials
🧪

Prospective Observational Pilot Study of LMWH Versus UFH as ECMO Anticoagulation in Lung Transplantation

Recruitingn/aAges 18 Years - anyAllUniversity Hospital, Motol
💬

In plain words

What the trial is, and whether it could suit you

The aim of this observational pilot study is to evaluate the effectiveness and safety of low-molecular-weight heparin (LMWH) compared to unfractionated heparin (UFH) as anticoagulation in perioperative ECMO during bilateral lung transplantation. The main question this study seeks to answer is: Does LMWH provide a safe and effective alternative to UFH for ECMO anticoagulation in lung transplantation, with reduced bleeding and thrombotic complications? Patients undergoing bilateral lung transplantation with perioperative veno-arterial (V-A) ECMO support will be assigned to one of two anticoagulation strategies: UFH group: Standard UFH anticoagulation monitored using ROTEM. LMWH group: Enoxaparin-based anticoagulation monitored using ROTEM. The study will assess perioperative blood loss, hemoglobin levels, transfusion needs, and thrombotic events. Additional analyses will include coagul

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: 1. ⃣ Adults (≥18 years old). 2. ⃣ Patients undergoing bilateral lung transplantation with perioperative veno-arterial (V-A) ECMO support. 3. ⃣ Planned perioperative anticoagulation with either UFH or LMWH, as determined by the attending anesthesiologist. 4. ⃣ Ability to provide informed consent or consent provided by a legally authorized representative. Exclusion Criteria: 1. ⃣ Patients receiving ECMO as a bridge to lung transplantation. 2. ⃣ Patients requiring postoperative continuation of ECMO. 3. ⃣ Patients with perioperative blood loss ≥3,000 mL. 4. ⃣ Patients undergoing lung re-transplantation. 5. ⃣ History of severe coagulopathy or bleeding disorder. 6. ⃣ Active use of antiplatelet or anticoagulant therapy (excluding study anticoagulants). 7. ⃣ Known heparin-induced thrombocytopenia (HIT). 8. ⃣ Severe liver dysfunction (Child-Pugh C) or end-stage renal disease requiring dialysis. 9. ⃣ Pregnant or breastfeeding women.
💊

What it tests

  • Not listed
📍

Where

1 site
University Hospital Motol, 2nd Faculty of Medicine, Charles University in Prague and 3rd Department of Surgery, First Faculty of Medicine, Charles University, and Motol University Hospital, Lung Transplant Program
Prague, Czechia
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
🛡️

AI Cure shows public evidence (Open Targets, ClinicalTrials.gov, PubMed, openFDA, DepMap, AlphaFold) with its source, and AI summaries that cite it — not medical advice and not a cure. Treatment decisions belong with your doctor. Research ideas are shared only with approved researchers and labs, who can test them. In an emergency call your local emergency number (112 in India and Europe, 911 in the US). AI Cure Terms of Use · Privacy