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Recruiting Observational

Sarcopenia, Metabolic Diseases, and Integrated Aging Longitudinal Evaluation (SMILE)

NCT07205510 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2020-12-01
Last updated
2025-10-03

Condition(s) studied

SarcopeniaMetabolic DiseasesAll-cause MortalityAgingCardiometabolic Diseases

Investigational drug(s) / intervention(s)

nothing

nothing: This is an observational study.

Study summary

This study aims to establish an ambispective cohort platform centered on the pathological axis of "sarcopenia-metabolic disorders-aging progression", integrating multimodal data including demographic characteristics, lifestyle factors, clinical phenotypes, laboratory tests, medical imaging, and biospecimens. Namely 'Sarcopenia, Metabolic Diseases, and Integrated Aging Longitudinal Evaluation (SMILE)'.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: Adults aged 18 and over Exclusion Criteria: 1. Does not cooperate in signing the informed consent form; 2. Does not possess legal capacity; 3. In a state of loss of consciousness; 4. Suffering from severe mental illness, unable to communicate normally; 5. The researcher believes that the subject has a disease that affects the assessment of results and is unsuitable for inclusion.

Primary outcome measure(s)

  • all-cause mortality — From enrollment to the 5-year and 10-year follow-up visit.
    Collect information on all-cause mortality of patients through hospital medical records, telephone follow-ups, outpatient follow-ups, etc., in order to assess the combined effects and underlying mechanisms of sarcopenia, metabolic diseases, and aging on all-cause mortality.

Trial sites (1)

FacilityCityRegionStatus
Department of Geriatrics, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China. Shanghai China Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07205510 on ClinicalTrials.gov ↗ ← All trials in China