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Study for serum concentration of posaconazole oral suspension for prevention of invasive fungal infection

Anti-fungal Exposure-Response Relationship in IFI

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026294
Enrollment
Unknown
Registered
2019-09-29
Start date
2017-03-24
Completion date
Unknown
Last updated
2019-10-14

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

Conditions

invasive fungal infection

Interventions

Case series:oral posaconazole 5ml, tid

Sponsors

hematology department of The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adult patients over 13 years of age with posaconazole for blood disease or hematopoietic stem cell transplantation. Blood diseases include aplastic anemia, acute myeloid leukemia, acute lymphocytic leukemia, non-hodgkin's lymphoma, multiple myeloma, or other blood tumor diseases; 2. Patients were expected to have or have documented persistent neutropenia (absolute neutropenia count (ANC) <= 0.5*10^9/L) and sustained for at least 7 days; 3. The patient or his authorized client agrees to participate in the clinical trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to posaconazole; 2. Patients without informed consent; 3. Any predictable increase in patient risk or other factors that can interfere with clinical trial results.

Design outcomes

Primary

MeasureTime frame
breakthrough infection after drug using;

Secondary

MeasureTime frame
Adverse Events;plasma concentration;absolute neutrophil count;duration of Agranulocytosis;

Countries

China

Contacts

Public ContactAining Sun

The First Affiliated Hospital of Soochow University

sunaining@suda.edu.cn+86 0512-67781856

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026