Health Condition 1: B44- Aspergillosis Health Condition 2: B37- Candidiasis Health Condition 3: B470- Eumycetoma Health Condition 4: B38- Coccidioidomycosis Health Condition 5: B45- Cryptococcosis Health Condition 6: B479- Mycetoma, unspecified
Conditions
Interventions
Intervention1: Nil: Nil
Intervention2: Nil: Nil
Intervention3: Nil: Nil
Intervention4: Nil: Nil
Intervention5: Nil: Nil
Sponsors
IPGMER and SSKM Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients attending OPD or admitted as inpatients of IPGMER and SSKM Hospital. The patients must be started on voriconazole within the last 3 days of screening by their treating physician and Participants must be willing to give informed consent for study participation.
Exclusion criteria
Exclusion criteria: Patients taking additional systemic antifungal drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To estimate the trough concentration of voriconazole in clinically suspected invasive fungal disease patients on day 3 to 5 of drug initiationTimepoint: Voriconazole trough concentrations between day 3 to day 5 and between week 3 to week 5 from drug initiation. Follow up at 8 weeks and 12 weeks from drug initiation | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effectiveness and safety along with clinical outcome in patients undergoing therapeutic drug monitoring of voriconazoleTimepoint: 18 months from incepton | — |
Countries
India
Contacts
Public ContactDr Suparna Chatterjee
IPGMER and SSKM Hospital
Outcome results
None listed