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:
2025-12-24 @ 11:40 PM
Ignite Modification Date:
2025-12-24 @ 11:40 PM
NCT ID:
NCT02244151
Eligibility Criteria:
Inclusion Criteria:
* Signed informed consent prior to carry out any procedure associated with the clinical trial.
* Women between 18 and 37 years of age at the time of randomization (both ages included).
Basal serum levels of FSH \<10 mIU /ml.
* Serum AMH \> 5 to \<45 pmol / l.
* Antral follicle count \> 6 and \< 24.
* Vaginal ultrasound documenting correct visualization of both ovaries and the absence of significant ovarian pathology.
* Short stimulation protocol with GnRH antagonist and conventional dose for ovarian stimulation with 225-300 UI of rhFSH.
* Number of follicles ≥ 16 mm \> 5 on the ovulation induction day.
Exclusion Criteria:
* Presence of severe endometriosis (Grade III-IV).
* Absence of one ovary due to previous surgery.
* Presence of significant uterine pathology (submucous myomas, endometrial polyp, malformations..)
* Diagnosis of polycystic ovary syndrome (defined according to the Rotterdam criteria).
* History of previous poor response to conventional ovarian stimulation protocols (\< 3 MII oocytes or canceled cycle)
* Severe male factor ( TMS\< 1 million).
* Participation in another RCT within the past one year.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
37 Years
Study:
NCT02244151
Study Brief:
Protocol Section:
NCT02244151