Skip to content

A Randomized Controlled Study on the Treatment of Diabetic Peripheral Neuropathy by Acupoint Injection of Shenfu Injection

A Randomized Controlled Study on the Treatment of Diabetic Peripheral Neuropathy by Acupoint Injection of Shenfu Injection

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011008
Enrollment
Unknown
Registered
2017-03-28
Start date
2017-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Diabetic peripheral neuropathy

Interventions

control group:Methycobal
treatment group:Shenfu injection
blood-letting therapy group :Shenfu injection+blood-letting therapy of ten finger-tip points

Sponsors

the first Affiliated Hospital of Sun Yat - sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. clear history of diabetes; 2. after diagnosis of diabetes or neurological disease; 3. clinical symptoms and signs consistent with DPN: such as the extremities paresthesia and (or) sensory disorder, limb loss or muscle atrophy, Toronto clinical scoring system (TCSS) score more than 6 points; 4. nerve electrophysiological examination abnormal lower limb motor nerve conduction velocity (MNCV) of less than 45 m/s, the sensory nerve conduction velocity (SNCV) < 40m/s; 5. aged 18 ~ 80 years old; 6. sexes; 7. agreed to accept the Chinese and Western medicine treatment.

Exclusion criteria

Exclusion criteria: Other factors (such as cerebrovascular disease, cervical disease, alcoholism, uremia, hypothyroidism, drugs) - induced peripheral neuropathy; is involved in other clinical trials; pregnant and lactating women; with severe pneumonia, pulmonary tuberculosis, lung abscess, myocarditis and other malignant tumor patients; heart, liver and kidney function serious damage (heart function from 3 to 4, ALT and / or AST more than 2 times the upper limit of normal, Cr more than the upper limit of normal); a mental illness, not very good cooperation; cannot obtain informed consent; researchers think that do not fit into the patients in the trial.

Design outcomes

Primary

MeasureTime frame
Neurophysiological detection;Toronto clinical scoring system;

Contacts

Public ContactJiuhui Liu

the first Affiliated Hospital of Sun Yat - sen University

liujiahui126@139.com+86 15989230877

Outcome results

None listed

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