Age-Related Macular Degeneration
Conditions
Brief summary
This prospective study will include about 40 patients with resistant wet age-related macular degeneration (AMD), diabetic macular edema (DME), or retinal vein occlusion edema (RVO) edema.The inclusion criteria are that all patients must be 40 years old or older, diagnosed with active wet AMD or macular edema due to RVO or DME, and have received at least four previous monthly injections of anti-VEGF other than faricimab. All patients will be switched to receive four loading doses of intravitreal faricimab (6 mg) at 4-week intervals for four months. The response to faricimab will be assessed regarding visual acuity and central macular thickness.
Detailed description
This prospective study will include about 40 patients with resistant wet age-related macular degeneration (AMD), diabetic macular edema (DME), or retinal vein occlusion edema (RVO) edema. The inclusion criteria are that all patients must be 40 years old or older, diagnosed with active wet AMD or macular edema due to RVO or DME, and have received at least four previous monthly injections of anti-VEGF other than faricimab. All patients will be switched to receive four loading doses of intravitreal faricimab (6 mg) at 4-week intervals for four months. The response to faricimab will be assessed regarding visual acuity (functionally), central macular thickness, and the presence of subretinal or intraretinal fluid (anatomically) by optical coherence tomography OCT and compared with pre-injection visual acuity and OCT.
Interventions
Faricimab (6 mg/0.05 mL) for three months (loading dose) in a sterile environment,
Sponsors
University of Baghdad
Study design
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
All patients enrolled in this prospective study were a sample of Iraqi patients diagnosed with resistant AMD, DME or RVO edema. These patients diagnosed as primary non-responders to Bevacizumab, Lucentis or Aflibercept.Eligible participants received monthly intravitreal injections of Faricimab (6 mg/0.05 mL) for three months (loading dose) in a sterile environment, following standard aseptic protocols. Patients observation and examination repeated after One month from the last injection to assess treatment response (BCVA, IOP and SD-OCT re-evaluation).The response to Faricimab was determined using both anatomical (CRT) and functional (BCVA) markers.
Eligibility
Sex/Gender
ALL
Age
45 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* 1\. Aged 45 years or older 2. DME, RVO edema, or wet-AMD diagnosed by clinical evidence and optical coherence tomography angiography (OCTA). 3\. Previously treated with: * At least six doses of Avastin in DME or RVO edema cases or 3 dose of Avastin in AMD cases in the last year. * At least five doses of Eylea in DME or RVO edema cases or 3 dose of Eylea in AMD cases in the last year. 4\. Lack of significant anatomical or visual improvement (i.e., primary non-responders) 5. Willingness and ability to attend follow-up appointments and comply with treatment protocol.
Exclusion criteria
* 1\. Inconsistent treatment history: missed a dose of anti-VEGF doses, or incomplete the three loading doses of Faricimab. 2\. Ocular comorbidities that could confound outcomes, such as: * Visually significant cataract as Grade 3+ or more. * Corneal opacity. * uveitis * Uncontrolled glaucoma (IOP \> 25 mmHg on meds) with an increase in cup/disc ratio. * Other macular pathologies (e.g., macular hole, epiretinal membrane ERM) 3. Severe baseline vision loss (BCVA \< 6/60).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| central retinal thickness | one month after the last faricimab injection | optical coherence tomography angiography |
Countries
Iraq
Outcome results
None listed