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 @ 4:59 AM
Ignite Modification Date:
2025-12-25 @ 4:59 AM
NCT ID:
NCT01223118
Eligibility Criteria:
This study will recruit patients from the NY/NJ/CT/eastern PA area only.
Inclusion Criteria:
1. No prior failed IVF treatment cycle
2. Female partner less than 35 years of age at time of onset of the IVF cycle
3. Normal maximum prior day 3 follicle stimulating hormone (FSH) level (\< or = 10 IU/L)
4. Total basal antral follicle count greater than or equal to 12
5. Male partner with greater than 100,000 total motile spermatozoa Donor sperm is acceptable but the couples will be required to provide one additional vial for DNA analysis
6. Body Mass Index (BMI) ≤ 32 kg/m2
Exclusion Criteria:
1. Diagnosis of chronic oligoovulation or anovulation (cycle typically occurring less often than every 38 days)
2. Diagnosis of endometrial insufficiency
3. Clinical indication for PGD (undergoing IVF with PGD to rule out a known genetic defect)
4. Use of testicular aspiration or biopsy procedures to obtain sperm
5. Unevaluated ovarian mass
6. Presence of hydrosalpinges which communicate with the endometrial cavity
7. Any contraindication to undergoing in vitro fertilization or gonadotropin stimulation
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT01223118
Study Brief:
Protocol Section:
NCT01223118