Does in Vivo Culture of Pre-cleavage Stage Embryo Reduce the Incidence of Aneuploidy?

Sponsor
Anecova SA (Industry)
Overall Status
Terminated
CT.gov ID
NCT02652143
Collaborator
(none)
35
1
2
5
7

Study Details

Study Description

Brief Summary

This Clinical Study has been designed to assess and compare the impact of in vitro or in vivo culture conditions on the euploidy of sibling blastocysts.

Condition or Disease Intervention/Treatment Phase
  • Device: AneVivo (Medical device for in vivo culture of embryos)
  • Other: comparator for embryo culture in vitro
N/A

Detailed Description

As soon as the very first minute of the fertilization process, very important biological events, critical for the future developmental competency of the embryo are taking place.

These biological events, after the sperm cell entry in the oocyte cytoplasm and prior to the first cleavage, include: the completion of the meiosis, the exclusion of the second polar body, the pronuclei formation, the replication of the male and female DNA and the chromosome segregation on the newly formed mitotic spindle.

If any of these events is aberrant, one or both of the two daughter cells and their descendants may carry chromosomal anomalies. In other words an uneven first cleavage in size or in content is associated with chromosomal abnormality and aneuploidy.

In vivo all these events occur in a natural environment where the presence of specific molecules and of a dynamic and physiological environment might be an advantage over in vitro culture conditions to ensure optimal cellular functions.

Preliminary data from the pilot study have shown a higher proportion of euploid embryos for sibling oocytes cultured in vivo vs. in vitro. Moreover, in animal models, in vivo cultured embryos have been described with significant reduction of aneuploidies and with differences in the gene expression levels patterns when compared to in vitro cultured embryos. There is also growing evidence that the culture conditions of human pre-implantation embryos can affect the gene expression regulation with measurable effects on embryos and on newborn children.

The investigators hypothesis is that in vivo produced embryos might have a higher percentage of euploidy when compared to their siblings cultured in vitro.

Study Design

Study Type:
Interventional
Actual Enrollment :
35 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Does in Vivo Culture of Pre-cleavage Stage Embryo Reduce the Incidence of Aneuploidy? A Sibling Oocyte, Prospective, Multi-centric, Randomized, Open Study, Clinical Study in Subjects With Subfertility Undergoing Assisted Reproductive Medical Treatment
Actual Study Start Date :
Jan 1, 2016
Actual Primary Completion Date :
Apr 1, 2016
Actual Study Completion Date :
Jun 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: sibling oocytes in vivo

randomized oocytes assigned to in vivo culture

Device: AneVivo (Medical device for in vivo culture of embryos)
Other Names:
  • Anecova
  • Active Comparator: sibling oocyte in vitro

    randomized oocytes assigned to in vitro culture

    Other: comparator for embryo culture in vitro

    Outcome Measures

    Primary Outcome Measures

    1. Euploidy status after a biopsy on all viable day 5 embryos [1 week]

      full genome analysis on 24 chromosomes

    Secondary Outcome Measures

    1. Implantation rate [9 weeks]

      number of gestational sac per transferred embryos

    2. Pregnancy rate [9 weeks]

      beating heart

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 38 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Signed Informed Consent by the subject and her partner

    • Women, aged between 18 and 38 years (up to 38th birthday)

    • ≤ 2 previous stimulation cycles

    • Routinely measured hormonal levels within normal range (i.e. FSH, LH, E2, PRL)

    • No uterine or ovarian anatomical abnormalities and/or alterations that would compromise device delivery or function in the uterus as demonstrated by ultrasound and trial insertion

    • 19 ≤ BMI ≤ 29 kg/m2

    Exclusion Criteria:
    • History of previous moderate or severe ovarian hyperstimulation syndrome (OHSS)

    • Severe endometriosis

    • Any active infection that would contraindicate ART, at the discretion of the investigator

    • Severe male factor in the partner (cryptozoospermia or non-obstructive azoospermia)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ivi Bilbao Bilbao Spain

    Sponsors and Collaborators

    • Anecova SA

    Investigators

    • Principal Investigator: Marcos Ferrando, MD, IVI Bilbao

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Anecova SA
    ClinicalTrials.gov Identifier:
    NCT02652143
    Other Study ID Numbers:
    • NCVd20H
    First Posted:
    Jan 11, 2016
    Last Update Posted:
    Apr 4, 2019
    Last Verified:
    Apr 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Anecova SA
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 4, 2019