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Therapeutic effect of mecobalamine in the sarcopenic elderly

Therapeutic effect of mecobalamine in the sarcopenic elderly

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113780
Enrollment
Unknown
Registered
2025-12-03
Start date
2025-12-10
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Sarcopenic

Interventions

Control group:Oral administration of placebo at the same dosage as the experimental group
Experimental group:Oral administration of methylcobalamin tablets 1 mg, three times a day

Sponsors

The Second Hospital University of South China
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Male aged 60 years or older (inclusive of the cutoff value) with independent ambulation ability; 2.Meeting the diagnostic criteria for sarcopenia (according to the 2019 Edition of the Asian Working Group for Sarcopenia Consensus on Diagnosis and Treatment): presence of decreased muscle strength (grip strength: male < 28 kg), reduced appendicular skeletal muscle mass (male < 7.0 kg/m^2, measured by dual-energy X-ray absorptiometry) and/or impaired physical function (6-meter gait speed < 1.0 m/s); 3.Stable health status; 4.Voluntarily agreeing to participate in the study and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Failure to meet the aforementioned diagnostic criteria and inclusion criteria; 2.History of allergy to methylcobalamin or any excipients in the formulation; 3.Engagement in work related to mercury and its compounds; 4.Presence of muscle disorders that may affect muscle mass and function, such as Duchenne muscular dystrophy, polymyositis, and myotonic dystrophy; 5.Other diseases that may affect muscle mass and function, such as vitamin B12 deficiency; 6.Resting systolic blood pressure > 200 mmHg or resting diastolic blood pressure > 100 mmHg; 7.Severe cardiac diseases: moderate to severe aortic stenosis, acute pericarditis, acute myocarditis, myocardial infarction, and uncontrolled arrhythmia; 8.History of acute stroke within the past 2 years; 9.Severe airway obstruction; 10.Lower limb fracture within the past 1 year or upper limb fracture within the past 6 months; 11.Hypercalcemia (corrected albumin serum calcium > 2.60 mmol/L); 12.Active malignant tumor; 13.Stage 4-5 chronic kidney disease; 14.Comorbidity of mental illness or moderate to severe cognitive impairment; 15.Long-term immobilization; 16.Other diseases that may interfere with the assessment of muscle mass, muscle strength, and physical function; 17.Inability to cooperate with treatment due to other reasons.

Design outcomes

Primary

MeasureTime frame
Grip strength;

Secondary

MeasureTime frame
Five-Times Sit-to-Stand Test;4-Meter Gait Speed Test;Standing Balance Test;6-Minute Walk Test;Appendicular Skeletal Muscle Mass Index;Four-Stage Balance Test;Short Physical Performance Battery Score;

Countries

China

Contacts

Public ContactWang Jianping

The Second Hospital University of South China

505142506@qq.com+86 139 7478 8927

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026