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 @ 1:43 AM
Ignite Modification Date:
2025-12-25 @ 1:43 AM
NCT ID:
NCT01599494
Eligibility Criteria:
Inclusion Criteria:
Please Note: In this trial an Indian female participant is defined as a woman 1) with native Indian parents, and 2) who is also in possession of an Indian identification card.
* Indian woman with an indication for COS and IVF/ICSI, but has not yet undergone IVF/ICSI.
* Body mass index (BMI) of 18.0 to 32.0 kg/m2
* Regular spontaneous menstrual cycle (ie, a menstrual schedule that consistently occurs within a range of 24 to 35 days)
* Access to available ejaculatory sperm. Use of donated and/or cryopreserved sperm is allowed, however sperm obtained via surgical sperm retrieval is not allowed.
* Results documented as 'within normal limits' from clinical laboratory tests (ie, complete blood count \[CBC\], blood chemistries, and urinalysis).
* Normal cervical smear result obtained within 12 months prior to study enrollment, otherwise test will be performed during screening.
* Able to adhere to dose and study visit schedules
Exclusion Criteria:
\- Has a recent (ie, within 3 years prior to enrollment in study) history of/or
any active endocrine abnormality, treated or untreated.
* Contraindicated use of gonadotropins
* History of ovarian hyper-responsiveness
* History of/or current polycystic ovary syndrome (PCOS)
* Has less than 2 ovaries or has any other ovarian abnormality, including endometrioma (greater than 10 mm in size), and/or has unilateral or bilateral hydrosalpinx and/or intrauterine fibroids (5 cm in size or greater), confirmed by an ultrasound scan.
* Has any clinically relevant pathology that may impair embryo implantation or continuation of pregnancy.
* Experienced more than three unsuccessful COS cycles for IVF/ICSI since
the last established ongoing pregnancy, if applicable.
* History of non- or low ovarian response to FSH and/or Menopausal Gonadotropin (hMG) treatment.
* History of recurrent miscarriage (ie, 3 or more)
* Positive test results for Human Immunodeficiency Virus (HIV) or
Hepatitis B
* Recent history of/or current epilepsy, thrombophilia, diabetes, cardiovascular, gastro-intestinal, hepatic, renal or pulmonary or auto-immune disease, any of which required or requires treatment.
* Smokes or recently stopped smoking (ie, within 3 months of study enrollment)
* History of/or active alcohol and/or drug abuse (ie, within 12 months prior to study enrollment).
* Previous use of corifollitropin alfa
* Use of hormonal agents known to affect ovulation or any drug/agent considered to be teratogenic
* Use of any experimental drug within 3 months prior to study enrollment or participation in another clinical study, other than one that is survey-questionnaire based.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
42 Years
Study:
NCT01599494
Study Brief:
Protocol Section:
NCT01599494