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Study on the safety and effectiveness of glucagon like peptide-1 in promoting the healing of diabetes foot ulcer

Study on the safety and effectiveness of glucagon like peptide-1 in promoting the healing of diabetes foot ulcer

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096850
Enrollment
Unknown
Registered
2025-02-07
Start date
2024-12-01
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

diabetic foot ulcers

Interventions

GLP-1RA(Liraglutide) therapy group:Routine dressing change is performed every 3 days, and GLP-1RA gel (liraglutide) is applied externally every day at a dose of 2ug/cm2/day
GLP-1RA(Loxenatide) therapy group:Routine dressing change every 3 days, and GLP-1RA gel (Losenatide) for external use every 7 days, with a dose of 1ug/cm2/week
Control group:Routine dressing change every 3 days

Sponsors

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. T2DM patients meet the diagnostic criteria of WHO1999; 2. DFU classification adopts Wagner I-II level; 3. Age over 18 years old; 4. The first-line routine treatment of diabetes wound did not heal for 4 weeks.

Exclusion criteria

Exclusion criteria: 1. DKA and hyperosmolar patients; 2. Patients with lower limb arterial occlusion or ABI<0.60; 3. Foot infection PEDIS grading 3-4; 4. Combine patients with severe coronary heart disease, cerebral infarction, heart failure, and renal failure; 5. Patients with malignant tumors, medullary thyroid carcinoma, and pancreatitis; 6. Patients with severe gastrointestinal diseases 7. using immunosuppressants; 8. Pregnant and lactating women. 9. Patients currently participating in other clinical trials; 10. Researchers believe that other reasons are not suitable for clinical trial participants.

Design outcomes

Primary

MeasureTime frame
Wound area;

Secondary

MeasureTime frame
capillary density;DFU treatment score;Regeneration degree of epidermis and granulation tissue;

Countries

China

Contacts

Public ContactShao Shiying

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology

shaoshiyingtj@163.com+86 13627144576

Outcome results

None listed

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