Clinical trial registry record

Basis: Evaluating Sirtuin Supplements To Benefit Elderly Trauma Patients (BES2T BET)

A registered PHASE1 study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Unknown.
Evidence
Registered phase 1 study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated January 6, 2020.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT03635411
Last registry update
January 6, 2020
Status
Unknown
Phase
Phase 1
Sponsor
Elysium Health
Enrollment
48
Countries
United States
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered PHASE1 study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase 1
Study design
RANDOMIZED · PARALLEL · OTHER · TRIPLE
Evidence population
Human clinical study registration
Participants
48
Population
ALL · 65 Years
Duration
2018-12-06 to 2020-12-01
Intervention
Nicotinamide Riboside and Pterostilbene; Placebo
Comparator
Placebo
Outcomes measured
Complications — 90 days; Grip Strength Scores — 90 days; Inhalation Volume Measurements — 90 days; 6 Minute Timed Walk Test Scores — 90 days; Timed Get Up and Go Test Scores — 90 days; Measurement of Muscle/ Fat Ratio — 90 days; Incidence of Adverse Events — 90 days; Incidence of Pain and Daily Pain Medication Dosage — 90 days; Analysis of Quality of Life Scores — 90 days; Late Life Function and Disability Instrument Scores analysis as a measure of subject independence, function, and disabi…; Analysis of scores on Mini Mental Status Exam as a measure of cognitive function and dementia — 90 days; Analysis of subject nutrition through Mini Nutritional Assessment Scores — 90 days; Analysis of Subject independence using Barthel Index scores — 90 days; Analysis of patient comorbidities as a measure of adverse events in evaluating Basis tolerability — 90 days; Analysis of inflammatory cell activity — 90 days; Analysis of Mitochondrial Function — 90 days
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.

Trial stage · Phase 1A trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

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.

  • Sirtuins · 100%Title contains controlled topic terminology. Summary contains controlled topic terminology. Title supplies ageing or longevity context.

Automated source check 100% · update recency 50%. These figures help sort records; they are not medical ratings.