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DTI evaluation of curative effect of acupoint injection at Zusanli on Type 2 diabetic peripheral neuropathy

DTI evaluation of curative effect of acupoint injection at Zusanli on Type 2 diabetic peripheral neuropathy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054566
Enrollment
Unknown
Registered
2021-12-20
Start date
2021-12-16
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

diabetes

Interventions

Experimental group:acupoint injection of mecobalamin at acupoint Zusanli
Control group:Mecobalamin intramuscular injection on hip muscle

Sponsors

Tianjin Medical University Zhu Xianyi Memorial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with type 2 diabetes; 2. Diabetic peripheral neuropathy with stable TCSS greater than 5; 3. Glycated hemoglobin greater than 7; 4. No nutritional neurological drugs have been used in the past 2 weeks; 5. Aged 18 to 60 years; 6. No lower extremity, knee joint trauma, surgery, and no release of nerve poisons.

Exclusion criteria

Exclusion criteria: 1. MR examination contraindications, cochlear implants, pacemakers and artificial stent implanters, claustrophobia; 2. Women who are pregnant, planning to become pregnant or breastfeeding; 3. Exclude the following diseases: (1) Cervical and lumbar spondylosis, infectious polyneuritis, chronic alcoholism, thyroid disease, drugs, poisoning, tumors, cerebrovascular sequelae, osteoarthritis, peripheral vascular disease, and peripheral neuropathy caused by genetics and other reasons: (2) Foot ulcer, infection and edema: (3) ABI<0.9; d) ALT and AST exceed 2 times the upper limit of normal, and serum creatinine exceeds the upper limit of normal. 4. Patients with severe organ diseases or combined with other serious primary diseases, mental illness, and patients with poorly controlled hypertension (blood pressure exceeds 160/100 mmHg after using antihypertensive drugs); 5. Patients with diabetic ketosis, ketoacidosis and severe infection within the past half month; 6. Those who have experienced bleeding or have bleeding tendency in the past 2 months; 7. Those with allergies: 8. The investigator believes that the patient is not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Toronto Clinical Neuropathy Score;Anisotropy of water molecules;Average degree of diffusion;

Countries

China

Contacts

Public ContactYu Wenjuan

Tianjin First Central Hospital

yuwenjuan2000@163.com+86 15022647334

Outcome results

None listed

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