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Comparison of Pulsed Radiofrequency and TENS on decreasing of Diabetic neuropathy symptoms in Lower extremity

Comparison of Pulsed Radiofrequency and Transcutaneous electrical nerve stimulation on decreasing of Diabetic neuropathy symptoms in Lower extremity in patients who did not respond to medications

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201212166186N1
Enrollment
60
Registered
2012-12-20
Start date
2012-12-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Diabetes mellitus. Diabetic autonomic neuropathy

Interventions

Intervention 1: for TENS group after cleaning the skin with alcohol, patch electrodes will be attached to the skin of lateral inferior part of knee and forfoot. then electrical impulses will be genera
Treatment - Devices
for TENS group after cleaning the skin with alcohol, patch electrodes will be attached to the skin of lateral inferior part of knee and forfoot. then electrical impulses will be generated with 80 Hz a
for RF group in operation room with fluoroscopic guide, the patient will be in prone position and RF needle will be inserted percutaneously from lumbar region to the lumbar sympathetic chain in antero

Sponsors

research office of anesthesiology and pain, guilan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criterion: diabetic patients who have been referred to the "Pain clinic" because of persistent pain and paresthesia in lower extremity who did not respond to oral medications. Exclusion criteria: coagulopathy; anti platelet and anticoagulant therapy; local infection at the procedure site; advanced stages of diabetic neuropathy without paresthesia and pain; addiction; cardiac pacemaker; epilepsy and pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before intervention, 7th day and 1st month and 3rd month after intervention. Method of measurement: numeric rating scale score.;Paresthesia. Timepoint: before intervention, 7th day and 1st month and 3rd month after intervention. Method of measurement: numeric rating scale score.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactbahram naderi nabi

guilan university of medical sciences

naderi_bahram@gums.ac.ir naderi_bahram@yahoo.com+98 13 1723 8889

Outcome results

None listed

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