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Clinical Study of Probiotics Intervention on Myopenia

Clinical Study of Probiotics Intervention on Myopenia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126991
Enrollment
Unknown
Registered
2026-06-22
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Interventions

Experimental group:The experimental group was treated with probiotics (two bags a day)
Control group:The control group was given probiotics-free powder with the same appearance as probiotics.

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 60 years; 2. Patients with sarcopenia meet the physical function assessment (gait speed < 1 m/s) and the measurement of DXA and BIA (male muscle mass < 7.0 kg/m^2 and female muscle mass < 5.7 kg/m^2); 3. Agree to participate in the experiment and cooperate with the visit, and sign the informed consent of the experiment.

Exclusion criteria

Exclusion criteria: 1. Chronic heart failure (NYHA III and IV), chronic kidney disease (CKD3-5 patients), chronic obstructive pulmonary disease (moderate and severe), neuromuscular diseases (ALS, SMA, inflammatory myopathy), rheumatoid arthritis, systemic lupus erythematosus and other CTD, long-term bed rest, post-stroke dyskinesia, long-term use of glucocorticoid, etc.; 2. Patients who have used antibiotics and/or probiotics in the past 4 weeks; 3. Patients who can't accept oral preparation treatment.

Design outcomes

Primary

MeasureTime frame
Skeletal muscle mass index of limbs;

Secondary

MeasureTime frame
Limb muscle mass;body fat percentage;

Countries

China

Contacts

Public ContactYanan Wei

Peking University People's Hospital

heye.wei@163.com+86 10 8832 6755

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026