IRCT20160221026674N5
Not Yet Recruiting
Phase 3
Investigating the added value of sensory retraining to duloxetine on pain, sensory symptoms, nerve conduction velocity, hand dexterity and static balance in patients with chemotherapy-induced sensory peripheral neuropathy- a controlled clinical trial study
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Shiraz University of Medical Sciences
- Enrollment
- 34
- Status
- Not Yet Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age over 40 years
- •Reporting the presence of symptoms of peripheral neuropathy including pain, numbness, tingling and any abnormal sensations by the patient
- •A score of at least 4 out of 10 in at least one of the symptoms of neuropathy in the numeric rating scale of pain in the hands and feet in the last week
- •Completion of the chemotherapy course of patients at least 3 months and at most 9 months before the start of the study and the existence of life expectancy for at least 6 months
Exclusion Criteria
- •The presence of other types of peripheral neuropathy before the start of chemotherapy
- •The presence of any wound or swelling in the treatment area (hands and feet)
- •Epilepsy or cardiac arrhythmia or the presence of a pacemaker in the patient's heart
- •Suffering from diabetes, hyperthyroidism, kidney failure, hepatitis, AIDS and vitamin B12 deficiency
- •Use of drugs such as Gabapentin and Pregabalin by patients during the study period
Outcomes
Primary Outcomes
Not specified
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