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
| Type | Name | Description |
|---|---|---|
| DRUG | Continuous infusion Linezolid | Linezolid 600 mg intravenous Loading dose followed by 1200 mg/ day by Continuous infusion ( 50 mg /hr ) |
| DRUG | intermittent dosing linezolid | Linezolid 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.