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Effects of long-acting GLP-1RA semaglutide on skeletal muscle mass in patients with liver cirrhosis and diabetes

Effects of long-acting GLP-1RA semaglutide on skeletal muscle mass in patients with liver cirrhosis and diabetes

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200067067
Enrollment
Unknown
Registered
2022-12-26
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

liver cirrhosis with diabetes

Interventions

observation group:Semaglutide 0.25mg, Qw start, step up to 1.0mg, Qw maintenance therapy
Control group 1 :Do not use semaglutide treatment, maintain the original hypoglycemic treatment regimen
Control group 2:Semaglutide 0.25mg, Qw start, step up to 1.0mg, Qw maintenance therapy
Control group 3:Do not use semaglutide treatment, maintain the original hypoglycemic treatment regimen

Sponsors

Beijing You'an Hospital ,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 18 = age < 65 years old, gender is not limited Clinical or pathological diagnosis of liver cirrhosis Child-Pugh A or B 7 points Definitely diagnosed as type 2 diabetes No anemia, HbA1c = 8.0% Newly diagnosed drug-free or hypoglycemic drugs have not been adjusted in the past 90 days, poor blood sugar control, need to use or switch to semaglutide Sign the informed consent

Exclusion criteria

Exclusion criteria: Family or personal history of multiple endocrine neoplasia type 2 or medullary thyroid carcinoma. Dependents are defined as first-degree relatives acute or chronic pancreatitis Existence or history of malignancy within 5 years prior to screening merged HIV History of diabetic ketoacidosis Myocardial infarction, stroke, unstable angina, or transient ischemic attack Coronary, carotid, or peripheral arterial revascularization eGFR less than 60ml/min/1.73m2 pregnancy Other patients considered unsuitable for this study by doctors, such as other serious diseases affecting nutritional status

Design outcomes

Primary

MeasureTime frame
L3-SMI;Blood glucose control;

Countries

China

Contacts

Public ContactZhang Jing

Beijing You'an Hospital ,Capital Medical University

zjyouan@ccmu.edu.cn13391859683

Outcome results

None listed

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