Clinical trial registry record

Effects of Shanyu Pill in Older Adults With Sarcopenia

A registered study indexed because it matched monitored longevity research terms. Registry status: Active Not Recruiting. 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 Active Not Recruiting.
Evidence
Registered phase not reported 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 September 4, 2026.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT05919368
Last registry update
September 4, 2026
Status
Active Not Recruiting
Phase
Phase not reported
Sponsor
Fujian University of Traditional Chinese Medicine
Enrollment
192
Countries
China
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

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

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · TRIPLE
Evidence population
Human clinical study registration
Participants
192
Population
ALL · 60 Years to 85 Years
Duration
2023-07-17 to 2026-12-10
Intervention
Shanyu pill; Placebo
Comparator
Placebo group
Outcomes measured
Change From Baseline in Appendicular Skeletal Muscle Mass Index (ASMI) — Baseline, Week 12, Week 24, and 2 years after…; Change From Baseline in Handgrip Strength — Baseline, Week 12, Week 24, and 2 years after completion of the 24-week int…; Change From Baseline in Five-Times Sit-to-Stand Test Performance — Baseline, Week 12, Week 24, and 2 years after comple…; Change From Baseline in Traditional Chinese Medicine Syndrome Score for Spleen Qi Deficiency — Baseline, Week 12, Week…; Change From Baseline in Gut Microbiota Composition — Baseline, Week 24, and 2 years after completion of the 24-week int…; Change From Baseline in Cortical Hemodynamic Responses Assessed by Functional Near-Infrared Spectroscopy — Baseline, We…; Change From Baseline in Gait Speed — Baseline, Week 12, Week 24, and 2 years after completion of the 24-week interventi…; Change From Baseline in 6-Minute Walk Distance — Baseline, Week 12, Week 24, and 2 years after completion of the 24-wee…; Change From Baseline in Short Physical Performance Battery Score — Baseline, Week 12, Week 24, and 2 years after comple…; Change From Baseline in Timed Up and Go Test Completion Time — Baseline, Week 12, Week 24, and 2 years after completion…; Change From Baseline in Montreal Cognitive Assessment Score — Baseline, Week 12, Week 24, and 2 years after completion…; Change From Baseline in Stroop Color-Word Test Completion Time — Baseline, Week 12, Week 24, and 2 years after completi…; Change From Baseline in Stroop Color-Word Test Accuracy — Baseline, Week 12, Week 24, and 2 years after completion of t…; Change From Baseline in Relative Abundance of Metabolites Detected by Untargeted Metabolomics — Baseline, Week 24, and…
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 not reportedA 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.

  • Sarcopenia · 100%Title contains controlled term: sarcopenia. Abstract contains controlled term: sarcopenia. Source terminology contains: sarcopenia. Title supplies longevity context: older adult. Study type is explicitly identified as INTERVENTIONAL.

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