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acetylcysteine in treatment of infertile women with polycystic ovarian syndrome

Phase 3
Conditions
Condition 1: infertility in polycystic ovarian syndrome. Condition 2: .
polycystic ovarian syndrome
Female infertility associated with anovulation
Registration Number
IRCT2014050617593N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
40
Inclusion Criteria

inclusion criteria: infertile women with PCOS (according to ESHRE/ASRM criteria) with normal hysterosalpingographies, normal spermograms of partners, and not impaired sexual functions
exclusion criteria: ovarian cyst >6 cm, history of asthma or allergy, consumption of any drugs with effects on glucose metabolism during the last 3 months before entering the trial.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ovulation rate. Timepoint: 7 days after intervention (14th day of menstrual cycle). Method of measurement: detecting at least one 18 mm follicle or larger in vaginal ultrasonography.;Pregnancy rate. Timepoint: 23 days after intervention (30th day of menstrual cycle). Method of measurement: laboratory measurement of hCG-ß level.
Secondary Outcome Measures
NameTimeMethod
Endometrial thickness. Timepoint: 7 days after intervention (14th day of menstrual cycle). Method of measurement: measuring endometrial thickness by means of vaginal ultrasonography (millimeters).
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