A registered PHASE3 study indexed because it matched monitored longevity research terms. Registry status: Recruiting. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase 3
- Study design
- RANDOMIZED · PARALLEL · TREATMENT · SINGLE
- Evidence population
- Human clinical study registration
- Participants
- 210
- Population
- ALL · 50 Years to 120 Years
- Duration
- 2021-04-16 to 2028-12-01
- Intervention
- Pars plana vitrectomy; Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until mon…; subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mls; Intravitreal 20% sulfahexafluoride (SF6) gas tamponade
- Comparator
- Arm B - Aflibercept monotherapy
- Outcomes measured
- assessment of Early Treat of Diabetic Retinopathy Study (ETDRS) letters of best-corrected visual acuity (BCVA) in the s…; Assessment of Early Treatment Diabetic Retinopathy Study (ETDRS) letter improvement in Best-Corrected Visual Acuity (BC…; Mean ETDRS BCVA — 6 and 12 months; Radner maximum reading speed — 6 and 12 months; Area of scotoma size using Humphrey Field Analyser 10-2 or equivalent — 6 and 12 month; National Eye Institute 25-item visual function questionnaire (NEI VFQ-25). composite score. — 6 and 12 months.; EQ-5D-5L with vision bolt-on score. — 6 and 12 months.; Presence/absence of subfoveal fibrosis and/or atrophy and area of fibrosis/atrophy using multimodal reading centre imag…
- Reported result
- No reusable finding-level result is available in this record.
Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.
Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.
Source supportStructured registry protocol metadata; no finding-level conclusion is generated.
Registration and recruitment status do not establish safety, efficacy, or regulatory approval.
Why this record appears here · 100% topic match
The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.
- Vision ageing · 100%Title contains controlled term: age-related macular degeneration. Abstract contains controlled term: age-related macular degeneration. Title supplies longevity context: age-related. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.
