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Clinical Trial Summary

Bleeding after thoracic surgery is a major cause of perioperative hemodynamic instability and transfusion requirement, which can lead to a rise of morbidity, mortality and costs.

The objective of this study is to evaluate the efficiency of tranexamic acid (TA) in the prevention of perioperative bleeding in thoracic hemorrhagic surgery.


Clinical Trial Description

It's a randomized, double-blind, prospective study including patients over the age of 18 years old, programmed for potentially hemorrhagic thoracic surgery, such as pulmonary resection for aspergilloma, pulmonary tuberculosis, pleural decortication, lobectomy with parietectomy or redux. Demographic, clinical, biological data as well as transfusion requirements, blood loss and perioperative complications were identified.

Two groups of patients:

- TA group: receiving tranexamic acid (25mg/kg) in bolus at induction followed by 2mg/kg/h in continuous infusion until the end of the act.

- Serum saline isotonic (SSI) group: placebo with isotonic saline serum. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04224116
Study type Interventional
Source University Tunis El Manar
Contact
Status Completed
Phase Phase 4
Start date January 1, 2014
Completion date October 2, 2019

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