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Factors on therapeutic drug monitoring and safety of voriconazole in critically ill elderly patients

Factors on therapeutic drug monitoring and safety of voriconazole in critically ill elderly patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097667
Enrollment
Unknown
Registered
2025-02-24
Start date
2023-12-22
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Invasive fungal infection

Interventions

the elderly group:NA
the non-elderly group:NA

Sponsors

Zhengzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.patients who met the criteria for diagnosis of IFI; 2.age >= 18 years; 3.The duration of voriconazole treatment course >= 5 days; 4.Draw at least one steady-state trough blood sample from each patient;

Exclusion criteria

Exclusion criteria: 1.Patients who allergic to voriconazole; 2.use other anti-fungal drugs; 3.pregnant or lactating women; 4.Hemodialysis patients; 5.patients who are treated with a combination of liver enzyme inducers and inhibitors (carbamazepine, phenobarbital, phenytoin, cimetidine, rifampin, rifapentine, rifabutin, and so on); 6.patients who haven’t completely and accurately data; 7.Participants in other clinical trials within 3 months;

Design outcomes

Primary

MeasureTime frame
Cmin;CYP2C19 genotypes;Alanine aminotransferase;Aspartate aminotransferase;Alkaline phosphatase;Total bilirubin;

Secondary

MeasureTime frame
C-reactive protein;Procalcitonin;Interleukin-6;

Countries

China

Contacts

Public ContactZhou Lijuan

Zhengzhou Central Hospital

zhou750423@126.com+86 13838014946

Outcome results

None listed

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