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
- NA · SINGLE GROUP · TREATMENT · NONE
- Evidence population
- Human clinical study registration
- Participants
- 30
- Population
- ALL · 50 Years to 99 Years
- Duration
- 2024-04-18 to 2026-05-15
- Intervention
- K8
- Comparator
- Not reported
- Outcomes measured
- Adverse Events — Within the study period (of 26 weeks); Mean change in best-corrected visual acuity (BCVA) — At baseline visit, week 13 visit, and week 26 visit; Mean change in low-luminance best-corrected visual acuity (ll-BCVA) — At baseline visit, week 13 visit, and week 26 vis…; Change in size of geographic atrophy (GA) on fundus autofluorescence (FAF) — At baseline visit, week 13 visit, and week…; change in size of geographic atrophy (GA) on optical coherence tomography (OCT) — At baseline visit, week 13 visit, and…; change in size of geographic atrophy (GA) on fluorescein angiogram (FA) — At baseline visit, week 13 visit, and week 26…; Change in multifocal electroretinograms (mfERG) response — At baseline visit, week 13 visit, and week 26 visit; Change in microperimetry response — At baseline visit, week 13 visit, and week 26 visit; Change in reading speed — At baseline visit, week 13 visit, and week 26 visit; Discontinued subjects — This will be done at every scheduled visit and any unscheduled visit, as well as when reported…; Change in best corrected visual acuity (BCVA) over multiple time points — Day 2 visit, Week 4 visit, Week 13 visit, Wee…
- 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%Abstract contains controlled term: age-related macular degeneration. Source terminology contains: age-related macular degeneration. Abstract supplies longevity context: aging, 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.
