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The effect of acupuncture on the symptoms of diabetes-related peripheral neuropathy (DPN).

Investigating the effect of acupuncture on the symptoms of diabetes-related peripheral neuropathy (DPN).

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181006041252N13
Enrollment
50
Registered
2019-06-27
Start date
2019-06-26
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Diabetes-related peripheral neuropathy (DPN).. Diabetes mellitus due to underlying condition with diabetic neuropathy, unspecified

Interventions

Intervention 1: Intervention group: The treatment group, in addition to routine therapies, will be treated with real acupuncture as a complementary therapy for seven sessions and once a week for 20 mi

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with their neuropathy are caused by type 1 and type 2 diabetes Patients with a pain score of 3 or more are in the form of an assessment of the visual scale of the pain. Patients aged 40 to 60 years. Patients with at least 10 years of diabetes.

Exclusion criteria

Exclusion criteria: Patients with diabetic foot ulcer Patients who drink alcohol or use tobacco. Patients who use immunosuppressive drugs have interfered with the interpretation of results. Patients whose neuropathy is caused by other disorders, such as carpal tunnel syndrome, AIDS, etc. Unwillingness to complete questionnaires and do acupuncture

Design outcomes

Primary

MeasureTime frame
Determine the amount of pain. Timepoint: Measuring the amount of pain at the beginning of the study (before the intervention) and at the end of each session for seven sessions (weekly) after the start of the intervention. Method of measurement: Visual Analogue Scale (VAS).

Secondary

MeasureTime frame
Determine fatigue. Timepoint: Fatigue measurement at the beginning of the study (before the intervention) and at the end of each session for seven sessions (weekly) after the start of the intervention. Method of measurement: Multidimensional Fatigue Inventory-20= MFI-20.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Sahebkar

Sabzevar University of Medical Sciences

Mohammad.Sahebkar66@gmail.com+98 51 4401 8337

Outcome results

None listed

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