Study for Obtaining Mature Oocytes by in Vitro Maturation in Oocyte-donor Women (IVM)

Instituto Valenciano de Infertilidad, IVI VALENCIA

Status: Completed

Conditions: Female Infertility

Treatments: Procedure: IN VITRO MATURATION AND OOCYTE ACTIVATION

Study type: Interventional

Funder types: Other

Identifiers

NCT03998553

1901-VLC-006-EB

Details and patient eligibility

About

In vitro maturation (IVM) is a technique for obtaining potentially fertilizable oocytes from immature oocytes. An oocyte must be mature both nuclearly and cytoplasmically in order to be competent in the reproductive process. Nuclear maturation involves an oocyte in metaphase II stage and is easily evaluated for its morphology. However, cytoplasmic maturation can only be evaluated by in vitro fertilization of that oocyte A mature nuclear and cytoplasmic oocyte is one capable of producing a viable embryo. This study aims to fine-tune the in vitro maturation (IVM) technique to achieve nuclear mature oocytes, i.e., to mature the oocytes up to the metaphase II stage. In addition, an artificial oocyte activation (AOA) will be carried out to check the cytoplasmic maturation of the oocytes, avoiding the generation of potentially viable embryos.

The aim of this study is to evaluate the response to the strategy stimulation with highly purified human menopausal gonadotropin (hMG-HP) administered for three days, in association with a standard methodology of in vitro oocyte maturation (IVM), to be performed on oocyte donors.

The correct functioning of this IVM technique would mean a reduction in the costs of ovarian stimulation treatments, as lower doses and shorter stimulation times are required, which implies lower risks for women derived from the medication and less stress for them.

Enrollment: 10 patients

Sex: Female

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Woman aged 18-35 years who have belonged to the egg donation program.
• Donors who agree to participate in the pre-trial report and sign informed consent.
• Good previous documented response to ovarian stimulation (at least 10 oocytes total and/or 8 MII).
• Donors with at least one previous cycle of donation, in which all the oocytes obtained were fertilized in fresh
• Patients who come to their last cycle of donation allowed by law
• No personal or family medical disorders history.
• Body mass index between 18-28 kg/m2
• Normal uterus and ovaries, without organic pathology
• Non-polycystic-looking ovaries
• Antral follicle Count (AFC) > 12 from both ovaries on day 2-3 of the menstrual cycle.
• Normal Karyotype
• Negative values of infectious diseases (hepatitis B virus, hepatitis C virus, human immunodeficiency virus and syphilis)
• Analytical with CBC, hemostasis and biochemistry with parameters within normality

Exclusion criteria

• Any systemic or metabolic disorder that counterindicates the use of gonadotrophins.
• Any medical condition involving non-inclusion in the oocyte donation program
• Who are taking hormonal contraceptives in the last 3 months
• Severe male Factor (Semen < 3 million)

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)