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Evaluation of the effects of lemongrass on clinical and electrodiagnostic symptoms of type 2 diabetes

Phase 3
Recruiting
Conditions
Type 2 diabetes.
Type 1 diabetes mellitus
Registration Number
IRCT20200612047739N1
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Type 2 diabetes
Age over 18 years
Body mass index 18.5–30 kg / m
Willing to participate in the study

Exclusion Criteria

Type 1 diabetes
Pregnancy or other specific types of diabetes
Insulin therapy over the past three months
Having serious gastrointestinal (GI) diseases including stomach ulcers and gastrointestinal bleeding
Having an autoimmune disease
Osteoarthritis
Chronic uremia
Use of drugs that affect the symptoms of neuropathy such as antidepressants and anticonvulsants
Allergy to Lemongrass

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical signs of neuropathy. Timepoint: Beginning and end of three months of treatment. Method of measurement: Physical examination.;Electrodiagnostic findings. Timepoint: Beginning and end of three months of treatment. Method of measurement: An electromyographic device will be used for this purpose.;Laboratory findings including Fasting blood sugar and hemoglobin A1c. Timepoint: Beginning and end of three months of treatment. Method of measurement: Based on laboratory evaluation of patients.
Secondary Outcome Measures
NameTimeMethod
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