Trials / Completed
CompletedNCT06124677
Single Injection of Faricimab for nAMD With Persisting Fluid Despite Frequent Aflibercept Treatments
Anatomical and Visual Outcomes Following a Single Injection of Intravitreal Faricimab in Patients With Neovascular Age-related Macular Degeneration and Persisting Fluid Despite Frequent Aflibercept Treatments
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 46 (actual)
- Sponsor
- Rigshospitalet, Denmark · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this retrospective single-center chat review is to establish the efficacy and safety of a single dose of intravitreal faricimab (Vabysmo®) injection in patients with neovascular age-related macular degeneration (AMD), who were previously treated with aflibercept (Eylea®) and had persisting intraretinal or subretinal fluid despite frequent treatments.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Faricimab | The Injections were performed according to local standard protocol, that included the use of 2-3 drops of topical tetracaine anesthesia, use of eye speculum, topical 5% povidone-iodine disinfection, a 30G-needle, injection site 3.5 mm posterior from the limbus marked by calipers in supertemporal or inferotemporal quadrants, a sterile cotton tip tamponade at the site of injection after removal of the needle, and no post-procedure antibiotics. |
Timeline
- Start date
- 2023-11-01
- Primary completion
- 2023-11-15
- Completion
- 2023-12-01
- First posted
- 2023-11-09
- Last updated
- 2023-12-11
Locations
1 site across 1 country: Denmark
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06124677. Inclusion in this directory is not an endorsement.