Skip to content

Continuous administration of linezolid: improving the dosage of an antibiotic

Linezolid continuous infusion: optimizing the dosage regimen in critically ill patients through a pharmacokinetic / pharmacodynamic analysis

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2015-002987-17-ES
Enrollment
Unknown
Registered
2015-11-05
Start date
2016-02-08
Completion date
Unknown
Last updated
2016-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infection

Interventions

Trade Name: Zyvoxid Pharmaceutical Form: Solution for infusion INN or Proposed INN: LINEZOLID Other descriptive name: LINEZOLID

Sponsors

Helena Barrasa
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Admitted to the intensive care unit. Diagnosis of sepsis. Need to linezolid because of suspected infection due to multiresistant gram positive cocci Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 15 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 10

Exclusion criteria

Exclusion criteria: Pregnancy. Age <18 years. Severe renal failure

Design outcomes

Secondary

MeasureTime frame
Secondary end point(s): To compare the risk of overexposure of two different dosage regimen of linezolid;Timepoint(s) of evaluation of this end point: 4 days

Primary

MeasureTime frame
Main Objective: To characterize the pharmacokinetics of linezolid when administered by continuous infusion;Secondary Objective: - To calculate the parameters related to the efficacy and toxicity - To cCompare the results with those obtained after conventional administration;Primary end point(s): To compare the efficacy of two different dosage regimen of linezolid;Timepoint(s) of evaluation of this end point: 4 days

Countries

Spain

Contacts

Public ContactUnidad de Cuidados Intensivos

Osakidetza

0034945007652

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026