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A Randomized Controlled Clinical Study on the Treatment of Early-Stage Diabetic Peripheral Neuropathy with 'Tonify Yin and Dredge Meridians' Electroacupuncture Therapy.

A Randomized Controlled Clinical Study on the Treatment of Early-Stage Diabetic Peripheral Neuropathy with 'Tonify Yin and Dredge Meridians' Electroacupuncture Therapy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002118
Enrollment
Unknown
Registered
2025-11-04
Start date
2025-11-05
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Diabetic peripheral neuropathy

Interventions

Intervention Group:Methylcobalamin + Electroacupuncture
Control Group:Methylcobalamin + Sham Needle

Sponsors

Beijing University of Chinese Medicine Oriental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosed with type 2 diabetes mellitus and meets the diagnostic criteria for diabetic peripheral neuropathy (DPN); (2) Receiving routine care for anti-hyperglycemic therapy with stable blood glucose control and glycated hemoglobin <8.5%; (3) Toronto Clinical Scoring System (TCSS) score =6 points; (4) Age between 20 and 75 years; (5) Normal understanding and communication abilities, able to cooperate with the study, and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with severe organic diseases such as heart, brain, liver, and kidney failure; patients with malignant tumors and mental illnesses; (2) Individuals who have experienced acute infections or acute complications of diabetes (diabetic ketoacidosis, hyperglycemic hyperosmolar state) within the past 3 months; (3) Patients with autoimmune system diseases; (4) Pregnant or breastfeeding women; (5) Individuals who have undergone acupuncture treatment within the past 6 months; (6) Participants in other clinical trials simultaneously; (7) Individuals who have taken methylcobalamin, epalrestat, or alpha-lipoic acid (used to treat diabetic peripheral neuropathy) within the past 4 weeks.

Design outcomes

Primary

MeasureTime frame
Toronto Clinical Neuropathy Scoring Scale (TCSS);

Secondary

MeasureTime frame
Nerve Conduction Velocity (NCV);Neuro Quantitative Sensory Examination;Quantitative Sensory Testing using Visual Analog Scale (VAS);Fasting Blood Glucose;glycated hemoglobin;

Countries

China

Contacts

Public ContactYi Wenming

Beijing University of Chinese Medicine Oriental Hospital

yiwenming33@sina.com13552439907

Outcome results

None listed

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