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The effect of cinnamon on polycystic ovarian syndrome

Not Applicable
Conditions
Polycystic ovary syndrome.
polycystic ovarian syndrome
Registration Number
IRCT2015121525537N1
Lead Sponsor
Vice chancellor for research,Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

informed consent to participate in the study? polycystic ovary syndrome diagnostic criteria Rotterdam are two of three of the following symptoms: i abnormal menstrual cycles (oligo dysmenorrhea, amenorrhea) ii polycystic ovaries on ultrasound iii clinical signs of hyperandrogenism (hirsutism -acne-) or biochemical signs of hyperandrogenism and also reject and Cushing's syndrome and congenital adrenal hyperplasia? age 45-18 years ?Body mass index (BMI) greater than or equal to 18.

Exclusion criteria:
any disease affecting variables (diabetes, liver disease, thyroid, cardiovascular, renal, gastrointestinal, Cushing's syndrome, adrenal hyperplasia, androgen-secreting tumors, hyperprolactinemia) based on the patient's previous history? Taking blood pressure medications or statins or anti-diabetic drugs and insulin injections ?Pregnancy ?Breast-feeding ?use of any vitamin supplements, minerals and hormones for at least two months before the study ?being under the special diet ?Consumers oral contraceptives (OCP), glucocorticoids, anti-androgens, ovulation induction drugs ?consumers of tobacco and alcohol ?a history of allergy to cinnamon

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Weight, body mass index, waist and hip. Timepoint: Before study and after 12 weeks. Method of measurement: questionnaire.;Fasting blood glucose, two hour blood glucose, serum insulin levels, lipid profile. Timepoint: Before study and after 12 weeks. Method of measurement: Blood sample.;Serum androgen levels. Timepoint: Before study and after 12 weeks. Method of measurement: Blood sample.
Secondary Outcome Measures
NameTimeMethod
The menstrual cycle regularity. Timepoint: Before study and after 12 weeks. Method of measurement: Questions from Patients.
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