Effect of Resveratrol and Pharmacist Intervention on Diabetes Mellitus and Its Neuropathic Complication
Diabetic Neuropathies
About this trial
This is an interventional treatment trial for Diabetic Neuropathies focused on measuring Diabetic neuropathy, Neuropathic pain, pharmaceutical care, Resveratrol
Eligibility Criteria
Inclusion Criteria:
- Patients with pain due to bilateral peripheral neuropathy caused by type 2 diabetes mellitus.
- HbA1c of greater than 7%
- A total symptoms score (TSS) of 7.5 points,
- The daily pain must be present for at least 6 months, and the diagnosis will be confirmed by a score of at least 3 on the Michigan Neuropathy Screening Instrument (MNSI). Patients had to have a mean score of ≥4 when assessed for 24-hour average pain severity on the 11-point Likert scale (from the patient diary prior to randomization).
Exclusion Criteria:
- Older subjects with high risks of cardiovascular diseases,
- Pregnant or breastfeeding,
- Having a prior renal transplant or current renal dialysis,
- Patients have a diagnosis of major depressive disorder, generalized anxiety disorder, heavy alcohol drinkers,
- Significant hepatic or renal disease,
- Patients on antioxidant therapy, or pentoxyphylline within the last month.
Sites / Locations
- College of Pharmacy-University of Sulaimani
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Placebo Comparator
Other
Other
Resveratrol
Placebo
Resveratrol plus Pharmaceutical care
Placebo with pharmaceutical care
Interventional group, participants in this group are receiving Resveratrol 500mg capsule once daily for 3 months.
Non-interventional group, participants are receiving only Placebo once daily for 3 months. Placebo formulated as capsule match the color and size of the active comparator,
Interventional group, participants in this group are receiving Resveratrol 500mg capsule once daily for 3 months with pharmaceutical care.
Interventional group, participants are receiving placebo along with pharmaceutical care for 3 months.