Congenital cytomegalovirus infection
Conditions
Interventions
oral VGCV at 32mg/kg/day (b.i.d) for 6 weeks
Sponsors
Department of Pediatrics, Nagoya University Graduate School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with congenital CMV-related SNHL or CMV-related clinical abnormalities other than SNHL
Exclusion criteria
Exclusion criteria: < 1 month of age < 32 weeks gestation < 1800g
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| auditory brainstem response | — |
Secondary
| Measure | Time frame |
|---|---|
| levels of CMV DNA in blood | — |
Countries
Japan
Contacts
Public ContactYoshinori Ito
Nagoya University Graduate School of Medicine Department of Pediatrics
Outcome results
None listed