Skip to content

pharmacokinetics and toxicity of linezolid in MDR-TB patients

pharmacokinetics and toxicity of linezolid in MDR-TB patients - Linezolid in MDR-TB

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29905
Enrollment
10
Registered
2006-09-28
Start date
2006-09-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

tuberculosis MDR-TB

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: MDR-TB attending physician initiates treatment with linezolid

Exclusion criteria

Exclusion criteria: allergy for linezolid

Design outcomes

Primary

MeasureTime frame
-Primary: PK of linezolid in MDR-TB patients

Secondary

MeasureTime frame
-Secondary: toxicity related to linezolid; i.e. anemia, and neurotoxicity

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)