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Experimental and clinical studies on intervention of lower extremity arteriosclerosis obliteration by Sichong tablet through regulation of TNF-NF-?b signal pathway

Clinical study of Sichong tablet in the treatment of lower extremity arteriosclerosis obliteration

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072544
Enrollment
Unknown
Registered
2023-06-16
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

lower extremity arteriosclerosis obliteration

Interventions

Treatment Group:Sichong tablet+Aspirin/Clopidogrel+ Rosuvastatin
Control Group:Aspirin/Clopidogrel+ Rosuvastatin

Sponsors

Jinan Municipal Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with lower limb arteriosclerosis obliterans (Rutherford stage 1) and voluntarily participating in the study by signing an informed consent form, aged between 18-75 years old.

Exclusion criteria

Exclusion criteria: (1) Patients who have had allergic reactions or adverse reactions to tetrahydropyranyl-tetrahydofurfuryl-naphthoic acid or other experimental drugs; (2) Patients with blood disorders such as coagulation dysfunction, anemia, platelet abnormalities, etc.; (3) Patients with bleeding disorders within the last 3 months; (4) Patients at high risk of major bleeding due to digestive ulcers, malignant tumors, esophageal varices, arteriovenous malformations, vascular aneurysms, etc.; (5) Patients with serious complications such as heart, brain, lung diseases, liver or kidney dysfunction; (6) Patients with inflammatory vascular diseases such as thromboangiitis obliterans, large-vessel vasculitis, or Raynaud's syndrome; (7) Pregnant and lactating women; (8) Patients with mental disorders; (9) Patients who are estimated by the investigator to have poor compliance and may have difficulty cooperating with treatment; (10) Patients with incomplete medical records.

Design outcomes

Primary

MeasureTime frame
Ankle brachial pressure index;

Secondary

MeasureTime frame
Blood lipid level;Skin temperature;Arterial blood flow parameters of lower limbs;The expression levels of TNF-a, IL-1ß, NF-?B p65, and I?Ba in peripheral blood;

Countries

China

Contacts

Public ContactWANG Yutao

Jinan Municipal Hospital of Traditional Chinese Medicine

jnwangyutao@163.com+86 152 7511 9546

Outcome results

None listed

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