Complicated nephrotic syndrome treated with rituximab
Conditions
Interventions
Influenza vaccines
Sponsors
Division of Nephrology and Rheumatology, National Center for Child Health and Development
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with complicated nephrotic syndrome who has been treated with rituximab in one year.
Exclusion criteria
Exclusion criteria: Patients who do not agree for the entry of the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MFI(mean fold increase) of GMT(geometric mean titer) of one month and three months after vaccination compared with that before vaccination. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Relationship between B-cell counts and MFI. 2) Relationship between period after the rituximab treatment and MFI. 3) Seroconversion rate of one month and three months after vaccination compared with that before vaccination. 4) Relationship between B-cell counts and seroconversion rate. 5) Relationship between period after the rituximab treatment and seroconversion rate. 6) Seroprotection rate of one month and three months after vaccination. 7) Relationship between B-cell counts and seroprotection rate. 8) Relationship between period after the rituximab treatment and seroprotection rate. 9) Relapses of nephrotic syndrome after vaccination. 10) Adverse events after vaccination. 11) Occurence of influenza infections. 12) Occurence of life-threatening influenza infections. | — |
Countries
Japan
Contacts
Public ContactKoichi Kamei
National Center for Child Health and Development Division of Nephrology and Rheumatology
Outcome results
None listed