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The effect of metformin on breast density

Phase 3
Recruiting
Conditions
Breast density.
Registration Number
IRCT20100706004329N9
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
146
Inclusion Criteria

Female gender
Age over 40 years

Exclusion Criteria

Suspicion of malignancy
Used of drugs that affect metabolic status, such as weight, glucose, and lipid-lowering agents During the study or three months before the study
History of breast cancer
Proven or suspected pregnancy and lactation during the intervention
Other medical conditions, such as cardiovascular disease, epilepsy, renal or hepatic disorders
Contraindications for metformin use (such as hypersensitivity to biguanides, acidemia, heart disease, alcohol consumption, gastroparesis, hepatic disease, hyperthyroidism or hypothyroidism, severe iron deficiency anemia, renal impairments)
History of unwanted and intolerable side effects of metformin (such as abdominal pain, chest pain, chills, cholestasis, diarrhea, dizziness, increased liver enzymes, severe headache, hepatitis, hypoglycemia, megaloblastic anemia, myalgia, nausea, Palpitations, rash, rash, vomiting)
Suffering from hormonal disorders and metabolic diseases such as hypo or hyperthyroidism, metabolic syndrome, diabetes, severe hyperlipidemia, galactorrhea

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Breast density. Timepoint: At the beginning of the study (before the intervention) and six months after the intervention. Method of measurement: Mammography scan.
Secondary Outcome Measures
NameTimeMethod
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