Actively Recruiting

Age: 20Years - 90Years
All Genders
Healthy Volunteers
NCT07334210

The Characteristics of Gut Microbiota in Patients With Sarcopenia and the Development of Probiotics

Led by Seoul National University Bundang Hospital · Updated on 2026-01-12

150

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary aim of this study is to identify the composition and characteristics of the gut microbiota in patients with sarcopenia in older adults, and compare these with the gut microbiota characteristics of older adults and young control groups to determine differences. Secondary purpose of this study is to provide data on the characteristics of gut microbiota for the development of probiotics effective in treating sarcopenia in older adults.

CONDITIONS

Official Title

The Characteristics of Gut Microbiota in Patients With Sarcopenia and the Development of Probiotics

Who Can Participate

Age: 20Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 65 to 90 years with sarcopenia diagnosed by 2019 AWGS guidelines including low muscle mass, low strength, or low physical performance
  • Individuals aged 65 to 90 years as older adult controls
  • Individuals aged 20 to 50 years as young adult controls
  • All participants must voluntarily agree and sign informed consent
Not Eligible

You will not qualify if you...

  • Currently receiving treatment for severe diseases of cardiovascular, immune, respiratory, gastrointestinal/hepatic and biliary, renal/urinary, neurological, psychiatric systems, infectious diseases, or malignant tumors (except non-melanoma skin tumors); cancer survivors only if less than 5 years remission
  • Difficulty with independent daily activities due to musculoskeletal or neurological diseases or cognitive impairment
  • Regularly consuming alcohol above WHO daily limits (≥40 g/day men, ≥20 g/day women)
  • Heavy smokers (≥20 cigarettes/day)
  • Elevated liver enzymes (AST or ALT ≥ 3 times upper normal limit)
  • Uncontrolled hypertension (systolic ≥ 140 mmHg or diastolic ≥ 90 mmHg after rest)
  • Uncontrolled diabetes mellitus (HbA1c > 7.0%)
  • Abnormal thyroid stimulating hormone levels (TSH ≤ 0.1 or ≥ 10 µIU/mL)
  • Deemed unsuitable by investigator for other reasons

AI-Screening

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Trial Site Locations

Total: 1 location

1

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, South Korea, 13620

Actively Recruiting

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Research Team

J

Jae-Young Lim

CONTACT

B

Bo-Ram Kim

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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