macular edema
Conditions
Interventions
an injection of 12mg or 20mg triamcinolone acetonide into the sub-Tenon capsule
Sponsors
the Department of Ophthalmology, University of Tokyo School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patient with macular edema
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Opptical coherence tomography findings (before and after 1 month and 3 months) and visual acuity (before and after 1 month and 3 months) | — |
Secondary
| Measure | Time frame |
|---|---|
| Intraocular pressure and cataract progression (before, after 1 week, 2weeks, 1 month, and 3 months), blood glucose level (daily, before and for 1week after injection), HbA1c (before and after 1 month and 3 months) and blood pressure (before and after 1 week) | — |
Countries
Japan
Contacts
Public ContactJunko Toda
University of Tokyo School of Medicine Department of Ophthalmology
Outcome results
None listed