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Clinical Trial Summary

- To identify the incidence of LIT among critically ill patients, as limited studies have only addressed this population. - To evaluate the impact of several factors on the incidence of LIT, the time to onset of LIT, and the time to recovery of platelets. - To study the effect of concurrent medications (enoxaparin, unfractinated heparin, piperacillin, carbapenems, tigecycline, fluconazole or voriconazole, digoxin, amiodarone, acetaminophen, tirofiban, statins, and antiepileptics) frequently used in critically ill patients on the incidence of LIT. - To investigate the impact of possible medications with an antioxidant effect on the prevention of LIT. - To assess the impact of LIT on composite end point (mortality, bleeding, and length of stay)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05944445
Study type Observational
Source Helwan University
Contact Amina S Adly, BCPS
Phone 00201559030055
Email Aminaosamaomar@gmail.com
Status Recruiting
Phase
Start date July 13, 2023
Completion date August 2024

See also
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