Description Module

Description Module

The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.

Description Module path is as follows:

Study -> Protocol Section -> Description Module

Description Module


Ignite Creation Date: 2025-12-25 @ 3:11 AM
Ignite Modification Date: 2025-12-25 @ 3:11 AM
NCT ID: NCT02802605
Brief Summary: Prospectively evaluation of the incidence of thromboembolic events in hospitalized cirrhotic patients. 2. Efficacy and safety of use of bemiparin in preventing peripheral and portal thrombosis. 3. Monitoring antiXa levels.
Detailed Description: PRIMARY OBJECTIVE: To evaluate the safety of prophylactic anticoagulation Bemiparina (HIBORĀ®) for the prevention of peripheral and portal vein thrombosis in cirrhotic patients with prolonged hospitalization. Secondary objectives are the following: 1. To evaluate the incidence of thrombotic events in hospitalized cirrhotic patients. 2. To evaluate the efficacy of low molecular weight heparin (HIBOR 3.500UI) in preventing thrombotic events in hospitalized cirrhotic patients. 3. To identify risk factors for development of portal vein thrombosis and deep vein thrombosis in hospitalized patients. 4. Evaluate the morbidity and mortality associated with thromboembolic events. 5. Evaluate prophylactic anticoagulation levels by determining antiXa and antithrombin III. 6. To study the expression profile and functionality of Toll-like receptors as factors intimately involved in the inflammatory response, as well as the variability of different serum markers associated with proinflammatory state: I-FABP / IL6-IL8 / NO, endothelin and LPS-binding protein. 7. Evaluate the effect on liver fibrosis (by FibroscanĀ®) and serum TGF 8. Evolution of hepatocellular function estimated by the scores of Child-Pugh and MELD.
Study: NCT02802605
Study Brief:
Protocol Section: NCT02802605