Impact of Parental Support on Pregnancy Outcomes (IPSO) Trial- Day 3 Preimplantation Genetic Screening (PGS) With Day 5 Fresh Transfer

Stopped early · Phase 4

Conditions studied: Preimplantation Gentic Screening (PGS), In Vitro Fertilization (IVF), Preimplantation Genetic Diagnosis (PGD)

In brief

Natera is recruiting patients for a research study evaluating pregnancy and implantation rates in women undergoing In Vitro Fertilization (IVF) and Preimplantation Genetic Screening (PGS). PGS is also referred to as Preimplantation Genetic Diagnosis (PGD) for aneuploidy. Healthy women undergoing IVF who are between the ages of 35 to 42 years are being recruited to participate in a randomized study. The purpose of this study is to determine whether PGS- testing of embryos created during IVF for chromosomal abnormalities, prior to transfer to the uterus- improves pregnancy and implantation rates in patients when compared to patients whose embryos are not tested. PGS will be conducted using 24 Chromosome Aneuploidy Screening with Parental Support from Natera. All subjects who qualify and enroll will receive discounted IVF medications (both TEST and CONTROL arms). If you become pregnant during the study, you will receive a small payment for providing information about your pregnancy and birth. If you are assigned to the TEST arm of the study you will receive free PGS.

Key facts

Study ID: NCT01194531
Run by: Natera, Inc.
People needed: 59
Starts: 2010-09-01
Expected to finish: 2013-04-01
Last updated by the study team: 2014-11-25

Who can join

Age: 35 and older, up to 42. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

Must agree to a follow-up visit at approximately 4-8 weeks gestation and a follow up phone call at 20 and 40 weeks gestation/livebirth. For patients assigned to the TEST group must agree to PGD testing and collection of buccal swab sample on newborn
At least 10 eggs retrieved
Must agree to use only Ferring products during stimulation
Normal uterine cavity detected on hysterosalpingogram (HSG), saline infusion sonogram (SIS), or hysteroscopy
Signed consent form

You may not qualify if…

FSH ≥10 IU/L within past year prior to screening
2 or more previously failed IVF cycles
Gestational or surrogate carrier, donor oocyte, donor sperm
History of recurrent pregnancy loss (3 or more consecutive miscarriages)
Severe male factor infertility defined as ejaculate sperm of < 1million sperm/ml, or sperm obtained through testicular biopsy
Gender selection as primary indication
Maternal disease that is not clinically stable and known to impact the ability to become pregnant or carry a pregnancy to term (lupus, chronic liver or kidney disease, body mass index (BMI) >35, uncontrolled hypertension, anti-phospholipid antibody, thrombophilia, insulin dependent diabetes)
Refusal or inability to comply with the requirements of the Protocol for any reason, including scheduled clinic visits and laboratory tests
Participation in any experimental drug study within 30 days prior to Screening
Prior hypersensitivity to any of the protocol drugs
Known history conveying increased risk for chromosome abnormality (beyond maternal age) or genetic disease in offspring

Where it is running

Huntington Reproductive Center — Laguna Hills, California, United States
Shady Grove Fertility RSC — Washington D.C., District of Columbia, United States
Florida Fertility Institute/ Women's Medical Research Group, LLC — Clearwater, Florida, United States
Atlanta Center for Reproductive Medicine — Atlanta, Georgia, United States
Fertility Centers of Illinois — Chicago, Illinois, United States
Boston IVF — Boston, Massachusetts, United States
The Nevada Center for Reproductive Medicine — Reno, Nevada, United States
Main Line Fertility — Bryn Mawr, Pennsylvania, United States
Fertility Specialist of Houston — Houston, Texas, United States

Full record on ClinicalTrials.gov

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