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Effect of propolis on diabetes mellitus

Phase 2
Conditions
type 2 diabetes.
Non-insulin-dependent diabetes mellitus
Registration Number
IRCT2014080218659N1
Lead Sponsor
Vice Chancellor for Research, Yazd Shahid Sadoughi University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
67
Inclusion Criteria

patients with type 2 diabetes mellitus, diagnosed 5-10 years ago, under treatment with oral hypoglycemic agents.
Exclusion criteria: pregnancy, lactation, insulin therapy, any other diseases such as autoimmune, intestinal, liver, thyroid and cardiovascular diseases, vitamin and mineral supplementation, history of dermal or digestive hypersensitivity to propolis, any severe respiratory disease (such as asthma, chronic bronchitis), report of side effects of propolis tablets.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fasting Blood Glucose. Timepoint: Before and after intervention. Method of measurement: Enzymatic method (mg/dl).;Fasting insulin. Timepoint: Before and after intervention. Method of measurement: ELISA(mU/l).;Triglyceride. Timepoint: Before and after intervention. Method of measurement: Enzymatic method (mg/dl).;Total cholesterol. Timepoint: Before and after intervention. Method of measurement: Enzymatic method (mg/dl).;LDL-C. Timepoint: before and after intervention. Method of measurement: Friedewald formula (mg/dl).;HDL-C. Timepoint: before and after intervention. Method of measurement: Precipitation(mg/dl).;Insulin resistance, sensitivity. Timepoint: Before and after intervention. Method of measurement: Software.
Secondary Outcome Measures
NameTimeMethod
HA1C. Timepoint: The baseline and three months after the intervention. Method of measurement: Turbidometry.
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