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

Last updated: July 13, 2023
Sponsor: Helwan University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Platelet Disorders

Thrombosis

Dysfunctional Uterine Bleeding

Treatment

Linezolid 600 mg

Clinical Study ID

NCT05944445
11041989
  • Ages > 18
  • All Genders

Study 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)

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

Exclusion

Exclusion Criteria:

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

Study Design

Total Participants: 310
Treatment Group(s): 1
Primary Treatment: Linezolid 600 mg
Phase:
Study Start date:
July 13, 2023
Estimated Completion Date:
August 31, 2024

Connect with a study center

  • 15 May hospital

    Cairo,
    Egypt

    Active - Recruiting

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