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Comparison of the effect of metformin versus acarbose and metformin in treatment polycystic ovarian syndrome patients

Not Applicable
Conditions
polycystic ovarian syndrome.
sclerocystic ovary syndrome
Registration Number
IRCT2013082214438N1
Lead Sponsor
Kermanshah University Of Medical Svience, Research Vice-Presidency
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
68
Inclusion Criteria

age 20-45 years; women with pcos diagnosed by the rotterdam consensus criteria (presence 2 of the following 3 conditions: a)oligomenorrhea /amenorrhea b)clinical or biochemical evidence of hyperandrogenism c)polycystic ovaries on sonography)
Exclusion criteria: patient with systemic disease such as cushing's syndrome; hyper or hypothyroidism; androgen secreting tumor; smokers; any systemic disease (liver ,renal,cardiovascular,diabet mellitus) ; receiving any drug for pcos such as aldacton,dian and clomiphen.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hirsutism. Timepoint: Before intervention - Four months after intervention. Method of measurement: Using Feriedman and Galway Scale.;Testostrone serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Serological test with Electr Komolomynsans method.;De Hydro Epi Andrestandion serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Serological test with Electr Komolomynsans method.;Fasting insulin serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Elysa asses.;Fasting sugar serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Enzyme.;Blood pressure. Timepoint: Before intervention - Four months after intervention. Method of measurement: Barometers.
Secondary Outcome Measures
NameTimeMethod
Triglycerid serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Serological test with Electro Komolynsans method.;Cholestrol serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Serological test with Electro Komolynsans method.;LDL serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Serological test with Electro Komolynsans method.;HDL serum level. Timepoint: Before intervention - Four months after intervention. Method of measurement: Serological test with Electro Komolynsans method.
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