IRCT20110413006186N13
Recruiting
Phase 2
A Comparison of the Effectiveness of Transcutaneous Electrical Nerve Stimulation and Duloxetine on Diabetic Peripheral Neuropathic pain
Rasht University of Medical Sciences0 sites60 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Rasht University of Medical Sciences
- Enrollment
- 60
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •patients type I or II diabetes mellitus, with diabetic neuropathic pain
- •Resistant to usual drug treatments, at least for 6 months
- •Minimum Pain Rating 4 based on Numerical Rating
- •Having normal creatinine and CBC blood counts
- •HBA1C less than 8%.
Exclusion Criteria
- •Having a pacemaker or defibrillator
- •Having brain stimulators
- •Infection or inflammation at the site of electrodes
- •Other neuropathies with causes other than diabetes
- •Alcohol consumption history
- •Malignant history
- •Tens Records history
- •Bipolar patients
- •Duloxetine contraindications such as liver or kidney failure and MAO\-I simultaneous use
Outcomes
Primary Outcomes
Not specified
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