Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:02 AM
Ignite Modification Date:
2025-12-25 @ 1:02 AM
NCT ID:
NCT03397693
Eligibility Criteria:
Inclusion Criteria:
* • Inclusion criteria of study group (1\&2):
1. Women with primary or secondary infertility for more than 1 year due to unexplained infertility (normal regular menstrual cycles and normal pelvic examination, evidence of ovulation by TV/US and/or normal mid-luteal serum progesterone, normal semen analysis of the husband according to WHO guidlines2010 (25), and evidence of tubal patency and normal uterine cavity by HSG and/or laparoscopy).
2. Women with PCOS according to Rotterdam ASRM/ESHRE criteria(26) • Inclusion criteria for control group (2):
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1. Women with no history of menstrual dysfunction or subfertility.
2. Normal regular cycles and normal pelvic examination.
3. Multipara with last delivery since ≥ 2 years with no history of abortions and not on contraception (hormonal or IUD).
Exclusion Criteria:
* • Exclusion criteria of both groups:
1. History of pelvic surgery or pelvic inflammatory disease.
2. Current hormonal contraception.
3. On IUD.
4. History of or clinical features suggesting endometriosis or pelvic pathology like uterine fibroid and ovarian cyst.
5. General medical disorders (e.g. D.M), smoking and lactation.
Sex:
FEMALE
Study:
NCT03397693
Study Brief:
Protocol Section:
NCT03397693