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Clinical efficacy of pentoxifylline in the treatment of chronic lower extremity arteriosclerosis obliterans in elderly patients with type 2 diabetes

Clinical efficacy of pentoxifylline in the treatment of chronic lower extremity arteriosclerosis obliterans in elderly patients with type 2 diabetes

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061096
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

diabetes and lower extremity arteriosclerosis obliterans

Interventions

Sponsors

Beijing hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 60 years; 2. Patients with type 2 diabetes (meeting the diagnostic criteria of the World Health Organization in 1999); 3. Clinical diagnosis of lower extremity arteriosclerosis obliterans, and the symptoms are not completely relieved by routine drug treatment (includes one of the following three situations, and the medication time >= 12 weeks: cilostazol 100 mg per time, twice a day; or salgrelide 100mg per time, three times a day; or beprostaglandin 40 ug per time, three times a day); 4. Meet one of the following standards: ABI = 50% in lower extremity artery by ultrasound, CT or MRI.

Exclusion criteria

Exclusion criteria: 1. Severe liver and kidney diseases; 2. Acute coronary syndrome and severe cardiac insufficiency; 3. Diabetic ketosis, ketoacidosis; 4. Acute infection; 5. Cancer patients; 6. Resting pain, foot gangrene and inability to walk; 7. Continuous blood pressure >= 160/100 mmhg; 8. Patients with bleeding related history such as gastrointestinal bleeding and retinal bleeding; 9. Patients unable to complete the study for other reasons.

Design outcomes

Primary

MeasureTime frame
Pain-free walking distance;Maximum walking distance;Ankle brachial index;Visual analogue scale;Paresthesia score;

Secondary

MeasureTime frame
Tumor necrosi factora;Interleukin-1;Interleukin-6;Matrix metalloproteinase 9;D-Dimer;High sensitivity C-reactive protein;Fibrinogen;

Countries

China

Contacts

Public ContactMou Zhongqing

Beijing Hospital

muzhongqing@126.com+86 13581857359

Outcome results

None listed

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