CClinicalTrials.gg
Status unknownNCT02662686MitoScoreUpdated Aug 8, 2018

Study for the Evaluation of "MitoScore" Marker in the Diagnosis of Embryo Viability in Euploids Embryos

An interventional study of Transfer according to morphological criteria and Transfer according to the MitoScore results in Infertility, sponsored by Igenomix. Status unknown at 11 sites in Spain. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2018-08-08.

Sponsored by Igenomix · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Aug 2018), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
1,718
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
Female
01

Study summary

The number of copies of mitochondrial genes (mtDNA or "MitoScore") is related to the energy supply of the embryo, which can affect its ability to implant in the maternal uterus.

The objective of this study is to analyse the potential of MitoScore before embryo transfer as a marker to identify and select the embryo with greater capacity of implantation. First of all, chromosomally normal embryos will be selected and mtDNA copies will be quantified. Finally, embryos with less copies of mtDNA will be considered for embryo transfer.

Read the detailed description

The number of mitochondrial DNA copies (mtDNA) of a chromosomally normal embryo is related to a state of energy, which affects the ability of the embryo to implant in the maternal uterus. There is a decrease in the rate of implantation in euploid embryos containing a high number of mtDNA copies. It is known that after a certain number of mtDNA copies implantation is disrupted even in euploid embryos.

The main purpose of this study is to evaluate the possible relationship between the mtDNA content contained in developing embryos and the result of implantation in order to evaluate the potential of such relationship as a diagnostic tool.

The number of mtDNA copies present in chromosomally normal embryos will be quantified. Subsequently, the transfer of euploid embryos after the randomization will be using either routine morphological or MitoScore criteria.

Study population: women undergoing either IVF or egg donation that go through preimplantation genetic screening (PGS) for different indications, either in day 5/6 or day 3.

This is a triple blinded, randomized, prospective, clinical study where patients with embryos analyzed by PGS in blastocyst stage or day 3 and mitochondrial analysis with day 5/6 transfer, with deferred cycle for those analyzed in day 5/6 and fresh embryo transfer for those analyzed in day 3, will be randomized into two groups:

GROUP A: Embryo selection for transfer will be based initially on chromosomal normality and secondly on embryo morphology criteria (specific for IVF lab).

GROUP B: Embryo selection for transfer will be based initially on chromosomal normality and secondly on the MitoScore value, trying to transfer normal embryos containing the lowest number of mitochondrial DNA copies.

02

Conditions studied

  • Infertility

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Keywords

  • Embryo Implantation
  • Mitochondrial genes
  • Mitochondrial DNA
  • MitoScore
  • Embryo selection
  • Embryo viability
  • Embryo biomarker
  • Diagnosis of embryo viability in euploids embryos
03

In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's planned enrollment of 1,718 is above the median of 120 across 1,698 interventional studies indexed under Infertility.

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Lead sponsor

Igenomix is the lead sponsor of 29 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • PGS cycles for different indications

    • Maternal age: ≤40 years old (FIV/ICSI patients)
    • Maternal age: \<50 years old (OVODON patients)
    • Spermatocyte concentration: > 2 million of spermatocyte/ml
    • Single embryo transfer

      -≥ 8 oocytes MII

    • Number of Antral Follicules (AFC: ≥10 MII)

Exclusion criteria

  • Detection in the moment of inclusion or previous diagnosis of congenital uterine malformations.

    • Patients with embryo sex selection for those countries in which it is allowed.
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
1,718 participants (estimated)

Study arms

  • Active comparator
    Control

    Embryo selection for transfer will be based initially on chromosomally normal embryos and secondly on embryo morphology criteria (specific of IVF lab, as standard practice).

    Other: Transfer according to morphological criteria

  • Experimental
    MitoScore

    Embryo selection for transfer will be based initially on chromosomal normality and secondly on the MitoScore value, trying to transfer chromosomally normal embryos which contain the lowest number of mitochondrial DNA copies.

    Other: Transfer according to the MitoScore results

Interventions

  • OtherTransfer according to morphological criteria

    Embryos will be analyzed by PGS and mitochondrial score on day 3 or day 5/6 biopsy and transferred on day 5/6, according to morphological criteria (control group).

  • OtherTransfer according to the MitoScore results

    Embryos will be analyzed by PGS and mitochondrial score on day 3 or day 5/6 biopsy and transferred on day 5/6, according to the MitoScore results (experimental group).

06

What researchers measure

Primary outcomes

  1. Implantation rate

    Time frame: 20 days

  2. Pregnancy rate

    Time frame: 12 days

Secondary outcomes

  1. Miscarriage rate

    Time frame: 9 months

  2. Ongoing pregnancy rate

    Time frame: 9 months

07

Study locations

11 sites
  • IVI Las Palmas
    Las Palmas de Gran Canaria, Las Palmas 35019, Spain
  • IVI Madrid
    Aravaca, Madrid 28023, Spain
  • IVI Bilbao
    Leioa, Vizcaya 48940, Spain
  • IVI Alicante
    Alicante, 03015, Spain
  • IVI Barcelona
    Barcelona, 08017, Spain
  • IVI Malaga
    Malaga, 29016, Spain
  • IVI Murcia
    Murcia, 30007, Spain
  • IVI Vigo
    Pontevedra, 35203, Spain
  • IVI Sevilla
    Sevilla, 41011, Spain
  • IVI Valencia
    Valencia, 46015, Spain
  • IVI Zaragoza
    Zaragoza, 50018, Spain
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 8, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02662686
Lead sponsor
Igenomix
Responsible party
Antonio Diez (Product Innovation Leader, Igenomix) — Principal investigator
First posted
Jan 25, 2016
Start date
Jan 2016
Primary completion
Dec 2018 (estimated)
Completion
Dec 2019 (estimated)
Last update
Aug 8, 2018

Study contacts

Antonio Diez, BS PhD
principal investigator · Igenomix
Carlos Simon, MD PhD
study director · Igenomix

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

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