Clinical Trials Directory

Trials / Unknown

UnknownNCT04531332

Continuous Infusion of Linezolid Versus Intermittent Dosing in the Treatment of Nosocomial Pneumonia

Efficacy and Safety of Continuous Infusion of Linezolid Compared With Intermittent Dosing in Critically Ill Pneumonic Patients

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
169 (estimated)
Sponsor
October 6 University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The investigator's goal in this study is to determine the clinical efficacy and safety of continuous infusion in comparison with standard intermittent infusion.

Detailed description

Prospective randomized controlled clinical trial on critically ill Pneumonic patients, included two groups, over one year period. The first group will be administered intravenous (IV) linezolid 600mg twice daily. The second group will be prescribed linezolid (IV) 600 mg loading dose followed by 1200 mg by continuous infusion. Both groups will be co-administered intravenous (IV) Meropenem 1g every 8 hours empirically.

Conditions

Interventions

TypeNameDescription
DRUGContinuous infusion LinezolidLinezolid 600 mg intravenous Loading dose followed by 1200 mg/ day by Continuous infusion ( 50 mg /hr )
DRUGintermittent dosing linezolidLinezolid 600 mg intravenous twice daily

Timeline

Start date
2019-11-15
Primary completion
2021-09-15
Completion
2021-09-15
First posted
2020-08-28
Last updated
2021-09-16

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04531332. Inclusion in this directory is not an endorsement.