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:
2026-03-26 @ 3:16 PM
Ignite Modification Date:
2026-03-26 @ 3:16 PM
NCT ID:
NCT07348757
Eligibility Criteria:
Inclusion Criteria:
* Women aged 20 to 43 years.
* BMI \< 30 kg/m².
* AMH \> 1 ng/mL.
* Undergoing IVF/ICSI treatment with a dydrogesterone-based PPOS protocol.
* Women with regular menstrual cycles or clinically acceptable cycle pattern for stimulation.
* Ability to provide informed consent and comply with study procedures.
* Presence of at least one ovary and eligibility for controlled ovarian stimulation
Exclusion Criteria:
* Cycle cancellation due to lack of viable embryos.
* Prior or planned PGT-A in the same cycle.
* Adenomyosis diagnosed by ultrasound or MRI.
* Uncorrected uterine anomalies (e.g., bicornuate, unicornuate, didelphys uterus).
* Presence of hydrosalpinx.
* Use of oral contraceptives or luteal-phase estradiol within 3 months before stimulation.
* Refusal or inability to provide informed consent.
* Severe systemic disease or contraindication to ovarian stimulation.
* Prior bilateral oophorectomy
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
43 Years
Study:
NCT07348757
Study Brief:
Protocol Section:
NCT07348757