Trials / Unknown
UnknownNCT02089503
Monocentric Retrospective Observational Study on Patients With Macular Degeneration
Monocentric Retrospective Observational Study Describing the Visual Acuity of Patients With Exudative Age Related Macular Degeneration and Treated by Lucentis® Under Real Conditions of Care.
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 250 (estimated)
- Sponsor
- Hospital St. Joseph, Marseille, France · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Main Objective: The main objective of this retrospective observational study was to describe the evolution of visual acuity measured on ETDRS (Early Treatment Diabetic Retinopathy Study) scale, for patients with exudative Age-Related Macular Degeneration (ARMD), treated with Lucentis, under real conditions of care, in terms of mean change of the Best Corrected Visual Acuity (BCVA), measured at 24 months (± 4 weeks).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | intravitreal injections of Lucentis | intravitreal injections FOR ALL PATIENTS of Lucentis as required in the normal condition of use |
Timeline
- Start date
- 2014-03-01
- Primary completion
- 2014-05-01
- Completion
- 2014-12-01
- First posted
- 2014-03-17
- Last updated
- 2014-03-18
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT02089503. Inclusion in this directory is not an endorsement.