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 · PREVENTION · DOUBLE
- Evidence population
- Human clinical study registration
- Participants
- 400
- Population
- ALL · 65 Years
- Duration
- 2024-04-01 to 2026-12-31
- Intervention
- Non-pharmacological intervention
- Comparator
- Control group
- Outcomes measured
- Postoperative delirum (POD) — : 10 minutes, 60 minutes, 120 minutes, 720 minutes and 1440 minutes after anesthesia; Frailty _FRAIL — Pre Anesthesia period at same day of the surgery; Frailty_CFS — Pre Anesthesia period at same day of the surgery; Screening of Cognitive impairment_MiniCog — Pre Anesthesia period at same day of the surgery; Possible Cognitive impairment_MoCA — Pre Anesthesia period at same day of the surgery; Risk of anesthesia — Pre Anesthesia period at same day of the surgery; Type of surgery — Pre Anesthesia period at same day of the surgery; Educational level of chile — Pre Anesthesia period at same day of the surgery; Type of Anesthesia — Up to 30 minutes after the end of the surgery; Electroencephalogram monitoring during the anesthesia — Up to 30 minutes after the end of the surgery; Type of drugs during anesthesia — Up to 30 minutes after the end of the surgery; Postoperative Pain — 10 minutes, 60 minutes, 120 minutes, 720 minutes and 1440 minutes after anesthesia; Positive POD Positive CAM: presence of post-operative delirium (POD) Negative CAM:. absence of postoperative delirium (…
- 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.
- Frailty · 100%Title contains controlled term: frailty. Abstract contains controlled term: frailty. Source terminology contains: frailty. Title supplies longevity context: frailty, frail. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.
