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Effects of melatonin supplementation in the treatment of fibrocystic breast disease

Phase 3
Conditions
breast fibrocystic disease.
Benign mammary dysplasia
Registration Number
IRCT20170513033941N59
Lead Sponsor
Kashan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Patients aged 18-45 years
women diagnosed with fibrocystic breast disease
having moderate or severe cyclic mastalgia
BMI = 25

Exclusion Criteria

Malignant breast diseases
Taking medicines for reducing pain (such as danazol, tamoxifen, bromocriptine) over the past three months
Menopause women
Pregnant or breastfeeding women
Psychological diseases
The consumption of any herbal or chemical sedative or hormonal medicines during the study
Unwillingness to cooperate

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Breast Pain Severity. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Visual analogue scale 0-10.;High-sensitivity C-reactive protein (hs-CRP). Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Elisa kit.
Secondary Outcome Measures
NameTimeMethod
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