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A case-control study on cardiopulmonary dysfunction in sarcopenia based on the theory of "the spleen governing qi and blood"

A Study on the Pathogenesis Evolution and Metabolic Regulation Mechanisms of Sarcopenia-Related Cardiopulmonary Dysfunction Based on the Theory of "Spleen Governing Qi and Blood"

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127300
Enrollment
Unknown
Registered
2026-06-29
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Cardiopulmonary Dysfunction Related to Sarcopenia

Interventions

Pre-sarcopenia group:None
Sarcopenia group:None

Sponsors

People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for participants in the pre-sarcopenia and sarcopenia groups (1)Participants who meet the diagnostic criteria according to the 2025 consensus update of the Asian Working Group for Sarcopenia; (2)Participants aged 50-80 years; (3)Participants who agree to participate in this study and provide written informed consent. 2.Inclusion criteria for participants in the non-sarcopenia group (1)Participants aged >=65 and 28 kg for males or >18 kg for females; participants aged >=50 and 34 kg for males or >20 kg for females; (2)Participants aged 50-80 years; (3)Participants who agree to participate in this study and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiac diseases, such as acute coronary syndrome within the past 6 months, implantation of a cardiac pacemaker, cardiac stent, or other metallic implants, or structural heart disease; 2. Patients with uncontrolled severe hypertension, such as systolic blood pressure >180 mmHg; 3. Patients with severe pulmonary diseases, such as severe chronic obstructive pulmonary disease, namely GOLD grade 3-4, interstitial lung disease, severe pulmonary infection, infectious pulmonary disease, asthma, or bronchiectasis; 4. Patients with severe brain diseases, such as cerebral hemorrhage or cerebral infarction; 5. Patients with severe liver diseases, such as liver cirrhosis or liver abscess; 6. Patients with severe kidney diseases, such as stage 5 chronic kidney disease or lupus nephritis; 7. Patients with a history of advanced malignant tumors; 8. Patients with hypoglycemia or acute diabetic complications; 9. Patients with severe hematological diseases; 10. Patients who have used glucocorticoids for a long time or at high doses; 11. Patients who have taken antibiotics or probiotics within the past 1 month; 12. Patients who have undergone major surgery recently, such as within the past 3 months; 13. Patients who have not provided informed consent, are unwilling to provide medical history information, or have incomplete data.

Design outcomes

Primary

MeasureTime frame
Pulmonary function test;Echocardiography;Electrocardiogram;N-terminal pro-B-type natriuretic peptide;Functional exercise capacity assessment;Arterial stiffness assessment;Chest digital radiography;Muscle strength;Muscle mass;Traditional Chinese medicine syndrome elements;Diaphragm ultrasound assessment;Limb skeletal muscle ultrasound assessment;

Secondary

MeasureTime frame
Laboratory test indicators;

Countries

China

Contacts

Public ContactHe Weidong

People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine

331312759@qq.com+86 158 8008 6382

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026