A registered 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 not reported
- Study design
- RANDOMIZED · PARALLEL · BASIC SCIENCE · QUADRUPLE
- Evidence population
- Human clinical study registration
- Participants
- 180
- Population
- ALL · 65 Years
- Duration
- 2025-04-17 to 2028-04-01
- Intervention
- Ketone ester; Placebo Comparator: Non-ketone placebo
- Comparator
- Ketone ester; Non-ketone placebo
- Outcomes measured
- Frailty composite score — Baseline, 12 weeks, 20 weeks; Tolerability key symptom index — 20 weeks; Safety Lab Tests — Baseline, Week 4, Week 12, 20 weeks; Leg fatigue - leg press at sub maximal weight — 20 weeks; Short Physical Performance Battery — Baseline, Week 12, 20 weeks; Grip Strength — Baseline, Week 12, Week 20; Montreal Cognitive Assessment — Baseline, 12 weeks, 20 weeks; Trails A and B — Baseline, Week 12, Week 20
- 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 · 80% 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.
- Frailty · 80%Title contains controlled term: frailty. Title supplies longevity context: aging, frailty. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.
