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Effect of Folic Acid Supplementation among Diabetic Polyneuropathy Patients

Early Phase 1
Conditions
Diabetic Polyneuropathy.
Type 2 diabetes mellitus with diabetic polyneuropathy
E11.42
Registration Number
IRCT20121216011763N22
Lead Sponsor
Vice chancellor for research, Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
80
Inclusion Criteria

>20 Years Old Diabetic Neuropathy Approved by the Neurologist Desire to Consume Folic Acid during 8 Weeks

Exclusion Criteria

Non-Diabetic Neuropathic Patients Pregnant Women Alcohol Users Smoking Multivitamin-minerals Containing Folic Acid, B12 and B6 Consumers during Study Drugs Consumers that may Interfere with the Absorption Folic Acid such as methotrexate, bacterium, antiepileptic and sulfa antibiotics

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
erve Conduction Velocity. Timepoint: week 0 and week 8. Method of measurement: EMG-NCV.;Serum folic acid. Timepoint: week 0 and week 8. Method of measurement: Laboratory analysis (blood test).;Serum vitamin B12. Timepoint: week 0 and week 8. Method of measurement: Laboratory analysis (blood test).;Serum homocystein. Timepoint: week 0 and week 8. Method of measurement: Laboratory analysis (blood test).
Secondary Outcome Measures
NameTimeMethod
CRP. Timepoint: Week 0 and week 8. Method of measurement: Laboratory analysis (blood test).;HbA1C. Timepoint: Week 0 and week 8. Method of measurement: Laboratory analysis (blood test).
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