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

H

Helwan University

Status

Enrolling

Conditions

Thrombocytopenia; Drugs

Treatments

Drug: Linezolid 600 mg

Study type

Observational

Funder types

Other

Identifiers

NCT05944445
11041989

Details and patient eligibility

About

  • 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)

Enrollment

310 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adult patients, age > or = 18 years old, admitted to the ICU with different indications.
  • candidates for intravenous linezolid therapy for > or =1 day.

Exclusion criteria

  • Taking any myelosuppressive drug.
  • Baseline platelets < 50000.
  • Patients with hematological malignancy.
  • COVID-19 patients.
  • Patients with immune thrombocytopenia

Trial design

310 participants in 1 patient group

Single arm group
Description:
Adult critically ill patients admitted to ICU for different indications
Treatment:
Drug: Linezolid 600 mg

Trial contacts and locations

1

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Central trial contact

Amina S Adly, BCPS

Data sourced from clinicaltrials.gov

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