drugset / Trial / NCT06285942

EdOxaban in fRagIle Patients With Percutaneous Endoscopic GAstrostoMy and atrIal fIbrIllation

NCT06285942

RandomizedParallel-groupSingle-blindTreatment

Summary

The goal of this interventional study is to describe the use of Edoxaban via PEG in patients with an indication to anticoagulation therapy. One arm will receive Edoxaban through PEG and the other arm will receive other Direct oral anticoagulants through PEG or subcutaneous heparin or LMWH. Once enrolled, patients will be treated with a single daily dose of Edoxaban (60 or 30 mg according to specific indications). At day 4 after enrollment (steady state), evaluation of anti-FXa activity and thrombin generation assay will be performed on peripheral whole blood samples. At months 6 and 12 patients will be asked to complete the ACTS (Anti-Clot treatment scale) questionnaire specific for anticoagulation. The main endpoint will be: the difference in the results of the Anti-Clot treatment scale questionnaire between the two groups evaluated at 12 months.

Timeline

Start
2024-02-01
Primary completion
2025-01-31
Completion
2025-01-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Edoxaban Small molecule 30 mg Other
Subject Edoxaban Small molecule 60 mg Other

Indications