MedPath

acetylcysteine and metformin in induction of ovulatio

Phase 3
Conditions
Polycystic ovary syndrome.
Polycystic ovary syndrome
E28.2
Registration Number
IRCT20210310050658N1
Lead Sponsor
Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
50
Inclusion Criteria

aged 20-35 years
infertile with polycystic ovary syndrome candidates for ovulation induction
spouse with normal sperm analysis
with normal hysterosalpingography without tubular pathology

Exclusion Criteria

Endocrine and endocrinological diseases such as thyroid disorders and abnormal prolactin
Patients who used metformin and clomiphene more frequently in the previous cycle to induce ovulation
Clomiphene resistant patients
Pituitary or hypothalamic disorders characterized by low gonadotropin levels
Drug allergy to metformin or N Acetyl Cystein
Simple ovarian cyst
Liver disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of follicles. Timepoint: Four weeks after the intervention. Method of measurement: Transvaginal ultrasound.;Endometrial thickness. Timepoint: Four weeks after the intervention. Method of measurement: Transvaginal ultrasound.;Size of follicles. Timepoint: Four weeks after the intervention. Method of measurement: Transvaginal ultrasound.;Frequency of intrauterine sac. Timepoint: Four weeks after the intervention. Method of measurement: Transvaginal ultrasound.
Secondary Outcome Measures
NameTimeMethod
Positive human chorionic gonadotropin (HCG). Timepoint: Four weeks after the intervention. Method of measurement: ELIZA test.
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