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Analysis of factors affecting elderly patients with diabetes mellitus combined with sarcopenia and intervention study of arginine combined with fish oil

Analysis of factors affecting elderly patients with diabetes mellitus combined with sarcopenia and intervention study of arginine combined with fish oil

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099259
Enrollment
Unknown
Registered
2025-03-20
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

sarcopenia

Interventions

Intervention group:Arginine+fish oil
Control group:placebo
Cross section (diabetes group):none

Sponsors

The 925th Hospital of the Chinese Joint Logistics Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: Cross-sectional study inclusion criteria: 1. over 60 years old, agreed to participate in the survey and signed informed consent; 2. Patients with diagnosed type 2 diabetes; 3. Can independently complete the body composition analysis and physical function test; Inclusion criteria for intervention research: 1. Over 60 years old, agree to participate in the survey and sign the informed consent; 2. Diagnosed patients with type 2 diabetes combined with sarcopenia; 3. Those who can eat orally and tolerate enteral nutrition; 4. can independently complete the body composition analysis and physical function test;

Exclusion criteria

Exclusion criteria: Exclusion criteria for cross-sectional studies: 1. Serious cognitive impairment, mental illness, etc., resulting in inability to participate in the test normally; 2. Patients with heart disease (including those equipped with pacemakers, heart stents), implant artificial joints, etc., who cannot participate in body composition tests and physical indicators tests; 3. Patients with severe dysfunction of heart, liver, kidney and other organs; 4. Refusing to cooperate with investigators. Exclusion criteria for intervention study: ? Patients with severe cognitive impairment or mental illness who could not normally participate in the test; ? Patients with heart disease (including those equipped with pacemakers, heart stents), implant artificial joints, etc., who cannot participate in body composition tests and physical indicators tests; ? Patients with severe dysfunction of heart, liver, kidney and other organs; ? Patients with dysphagia; ?Long-term use of thyroid drugs, steroids and estrogen and other drugs; ? Poor compliance and study doctors deemed unsuitable candidates; ? Patients with severe sepsis or systemic inflammatory response syndrome.

Design outcomes

Primary

MeasureTime frame
6m pace;Serum insulin;Triglyceride-glucose index;SMI;Calf circumference;grip;glut4 glucose transporter;NO;Fasting blood glucose;2h postprandial blood glucose;HOMA-IR;SARC-CALF;

Secondary

MeasureTime frame
Length of hospitalization;Number of readmissions within one year;

Countries

China

Contacts

Public ContactYuan Lijia

The 925th Hospital

2394718057@qq.com+86 198 2125 6518

Outcome results

None listed

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