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The effect of Nigella Sativa on oligomenorrhea and amenorrhea in patients with polycystic ovary syndrome

Not Applicable
Conditions
Polycystic ovarian syndrome.
Polycystic ovarian syndrome
Registration Number
IRCT2016041827455N1
Lead Sponsor
School of Traditional Medicine, Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
68
Inclusion Criteria

Diagnosis of Polycystic Ovary syndrome by gynecologist, according to the National Institute of Health’s criteria; women aged 18-38 years old with irregular periods; having informed consent; Non-consumer of any hormonal medication and Metformin for at least three months prior the study.
Exclusion criteria: Using anti-hypertensive, anti-cholesterol, anti- diabetic, insulin-sensitizing,medication; using aspirin and other anti-clotting medications, oral contraceptive and the anti-prostaglandin medications, parallel consumption of other herbal medications for disease treatment; patient with uncontrolled high blood pressure history, brain stroke, heart attack, cancer, cardiovascular disorders, liver disease, renal and thyroid disorders, type 1 or 2 diabetes; pregnancy and lactation; smoking.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
0ccurance of Menstrual bleeding. Timepoint: Before the intervention,1, 2, 3 and 4 months after the intervention. Method of measurement: Ask the patient.;Duration of menstural bleeding. Timepoint: Before intervention and 1,2,3, 4 month after intervention. Method of measurement: Ask the patient and complete tracking form.;Menstrual blood volume. Timepoint: Before intervention and1,2, 3, 4 month after intervention. Method of measurement: Pictorial Blood Loss Assessment Chart (PBAC).
Secondary Outcome Measures
NameTimeMethod
Menstrual cycle length. Timepoint: Before intervention and1,2, 3, 4 month after intervention. Method of measurement: Ask the patient and complete tracking form.;Serum LH. Timepoint: Before intervention and 3 month after intervention. Method of measurement: Serum analysis by ELIZA.;Total Testosterone. Timepoint: Before intervention and 3 month after intervention. Method of measurement: Serum analysis by ELIZA.
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