Kala-azar (visceral leishmaniasis) and post-kala-azar dermal leishmaniasis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who visit the participating facilities and are diagnosed with kala-azar (visceral leishmaniasis) or post-kala-azar dermal leishmaniasis
Exclusion criteria
Exclusion criteria: Patients who refuse to participate in this observational study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Short- and long-term patient outcomes (1 month to 3 years) by treatment plan, especially the onset of post-kala-azar dermal leishmaniasis | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Details of patient background, history, subjective symptoms, and objective findings at the time of diagnosis 2.Assessing the diagnostic effectiveness of serum and urine biomarkers | — |
Countries
Asia(except Japan)
Contacts
The University of Tokyo Hospital Department of Hemodialysis and Apheresis