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The effect of oral Clonidine on the treatment of diabetic neuropathy.

Phase 2
Recruiting
Conditions
Diabet- Diabetic neuropathy..
Type 2 diabetes mellitus with diabetic neuropathy, unspecified.
E11.40
Registration Number
IRCT20211106052983N1
Lead Sponsor
Yasouj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Patients with type 2 diabetes who have symptoms associated with peripheral neuropathy.
No chronic illness (cardiovascular, renal and thyroid disorders), severe neurology or psychiatry.
Do not be pregnant or breastfeeding.
Not taking medications that are effective in exacerbating or alleviating neuropathy.
Age between 30 and 60 years old.

Exclusion Criteria

Having severe sensitivity to Clonidine
Having neuropathy with proven reasons except Diabetes

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of neuropathy in this study based on the Michigan Questionnaire, pain based on the McGill Pain Questionnaire. Timepoint: Before the start of the study and 14, 28, 56 days later. Method of measurement: The Michigan Questionnaire, the McGill Questionnaire, and the researcher-designed questionnaire.
Secondary Outcome Measures
NameTimeMethod
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