Skip to content

Randomized double-blind placebo-controlled study of Wentong Huoxue cream in the treatment of diabetes peripheral neuropathy

Randomized controlled study of Wentong Huoxue cream in the treatment of diabetes peripheral neuropathy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078843
Enrollment
Unknown
Registered
2023-12-19
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Diabetes peripheral neuropathy

Interventions

Intervention group:Wentong Huoxue Cream+Basic Treatment
Control group:Wen Tong Huo Xue Cream Simulator+Basic Treatment

Sponsors

Xinjiang Uygur Autonomous Region Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age range from 18 to 75 years old; (2) Patients with type 2 diabetes peripheral neuropathy; (3) Voluntarily participate in this experiment and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Toronto score = 5 points (2) Other neurological disorders, such as cervical or lumbar spondylosis (nerve root compression, spinal stenosis, cervical and lumbar degenerative changes), cerebral infarction, Guillain Barre syndrome, or severe arteriovenous disease (venous thrombosis, lymphangitis) (3) Patients with lower limb skin ulcers or gangrene, moderate to severe edema of the lower limbs, or those with lower limb skin diseases; (4) Acute complications such as diabetes ketoacidosis, hyperglycemia and hypertonic syndrome, diabetes lactic acidosis, and acute gout patients; (5) Patients with malignant tumors or severe heart, liver, and kidney dysfunction; (6) Pregnant or lactating individuals, or those who have planned to conceive within the past year; (7) Participants in other clinical studies within the past three months; (8) Those who cannot understand the nature, scope, and possible outcomes of the research or cannot follow medical advice; (9) Individuals with allergic constitution and a history of drug, food, and contact allergies.

Design outcomes

Primary

MeasureTime frame
Toronto Clinical Scoring System;VAS ;

Secondary

MeasureTime frame
Changes in nerve electrophysiological conduction velocity;Vibration perception threshold;TCM symptom rating scale;ABI ;

Countries

CNINA

Contacts

Public ContactMA LI

researcher

majing13579200395@foxmail.com+86 136 9998 3028

Outcome results

None listed

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