Clinical Trials Directory

Trials / Unknown

UnknownNCT05944445

The Incidence of Linezolid-induced Thrombocytopenia (LIT) in Critically Ill Patients, the Risk Factors for LIT

The Incidence of Linezolid-induced Thrombocytopenia (LIT) in Critically Ill Patients, the Risk Factors for LIT and Time to Events (LIT, Recovery)

Status
Unknown
Phase
Study type
Observational
Enrollment
310 (estimated)
Sponsor
Helwan University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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)

Conditions

Interventions

TypeNameDescription
DRUGLinezolid 600 mgLinezolid 600mg injection

Timeline

Start date
2023-07-13
Primary completion
2024-08-01
Completion
2024-08-01
First posted
2023-07-13
Last updated
2023-07-17

Locations

1 site across 1 country: Egypt

Regulatory

Source: ClinicalTrials.gov record NCT05944445. Inclusion in this directory is not an endorsement.