A registered PHASE1, PHASE2 study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase 1, Phase 2
- Study design
- RANDOMIZED · PARALLEL · TREATMENT · NONE
- Evidence population
- Human clinical study registration
- Participants
- 88
- Population
- ALL · 50 Years
- Duration
- 2005-04-01 to 2009-01-01
- Intervention
- Ranibizumab
- Comparator
- Not reported
- Outcomes measured
- Mean Change From Baseline in the Best Corrected Visual Acuity Score of the Study Eye at Month 6 in Group B — Baseline a…; Mean Change From Baseline in the Best Corrected Visual Acuity Score of the Study Eye at Month 12 in Group B — Baseline…; Categorical Analysis of Best Corrected Visual Acuity of the Study Eye at Month 6 and Month 12 in Group B — Baseline, Mo…; Extension Phase: Mean Change From Month 12 (Start of Extension Phase) in Best Corrected Visual Acuity Score of the Stud…; Extension Phase: Categorical Analysis of Best Corrected Visual Acuity of the Study Eye at Last Visit of Extension Phase…; Mean Change From Baseline in Total Area of Choroidal Neovascularization of the Study Eye in Group B — Baseline, Months…; Mean Change From Baseline in Total Area of Leakage From CNV Plus Staining of Retinal Pigment Epithelium of the Study Ey…; Percentage of Participants in Group B With Absence of Leakage in the Study Eye at Month 3, 6, 9 and 12. — Months 3, 6,…; Mean Change From Baseline in Foveal Retinal Thickness of the Study Eye in Group B — Baseline, Months 3, 6, 9 and 12; Mean Change From Baseline in Total Retinal Volume of the Study Eye in Group B — Baseline, Months 3, 6, 9 and 12
- 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 topic terminology. Summary contains controlled topic terminology. Source terminology contains a controlled topic term. Title supplies ageing or longevity context.
Automated source check 100% · update recency 35%. These figures help sort records; they are not medical ratings.
