In Vitro Maturation of Human Eggs (IVM)

National Foundation for Fertility Research

Status

Unknown

Conditions

Reproductive Techniques, Assisted

Infertility

Treatments

Device: IVM media

Drug: Follicle Stimulating Hormone (FSH)

Study type

Interventional

Funder types

Other

Identifiers

NCT02516462

NFFR-IVM-2015

Details and patient eligibility

About

Because a large proportion of the embryo's quality is dependent upon the egg, this investigation focuses on treatment of the oocyte during in vitro maturation (IVM). In typical IVF cycles, the egg is recovered when it is mature and ready to be fertilized. However, at this point the oocyte's quality has been set, and cannot be altered. Therefore, to have an impact on oocyte quality the use of in IVM is critical. Development of a successful IVM protocol for clinical use would not only provide an option for women of advanced maternal age, it would also reduce the cost of IVF due to fewer exogenous gonadotropins used for stimulation, and significantly lessen the risk of ovarian hyper-stimulation.

The objective of this research study is to evaluate a newly developed oocyte maturation media system for human clinical use in assisted reproductive technology (ART).

Full description

The novel device (IVM media system), is designed to support nuclear maturation of immature oocytes recovered after minimal ovarian stimulation with no LH/hCG administration, and improve oocyte competence. This may result in development of a greater number of embryos to the blastocyst stage.

FSH is administered starting on cycle day 3 to stimulate follicle growth. When the leading follicle reaches 12-14 mm, egg retrieval will be scheduled. No hCG/LH trigger will be administered. Specially designed maturation media is used to collect and culture the immature eggs once recovered from the follicle. Once the eggs have matured in vitro, fertilization and embryo culture, vitrification and comprehensive chromosomal screening will be completed as per standard operating procedures.

Enrollment

100 estimated patients

Sex

Female

Ages

21 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Infertile women who desire to conceive and come to CCRM for infertility treatment using IVF will be candidates for this study.
Women with PCOS
Patients can be of any race, culture, sexual orientation or ethnicity.

Exclusion criteria

Minors are excluded from participation in this study.
Women with a BMI greater than 40
Women whose health is such that becoming pregnant carries risk significantly greater than healthy women are excluded from this study, unless they use a gestational carrier under the direction of their physician.