Interest of Morphokinetic Parameters of Early Embryonic Development in the Birth Rates in Vitro Fertilization
EMCIMO
Do the Morphokinetic Parameters of Early Embryonic Development Have an Interest in the Choice of the Embryo to be Transferred and Improve Birth Rates in Vitro Fertilization
1 other identifier
interventional
520
1 country
2
Brief Summary
In France, nearly 3% of children are conceived by the technique of Assisted Reproductive Medicine, of which nearly 70% by in vitro fertilization (IVF). The rates of clinical pregnancy by oocyte retrieval or embryo transfer have not changed much. The use of mono-embryo transfer reduces the risk of multiple pregnancies and associated obstetric complications. The choice of embryo to transfer or freeze is a key element in improving the chances of success of IVF. It is usually based on conventional morphological criteria (reference method) that are punctual, qualitative and subjective. However, embryo morphology at early stages has little predictive value for obtaining a late-stage embryo and its chances of implantation. The recent use of time-lapse technology during embryonic culture makes it possible to associate morphological criteria with continuous monitoring of the kinetics of embryonic development. The choice of the embryo to be transferred is then made according to morphokinetic criteria (conventional morphological criteria to which are added the data of the kinetics of embryonic development). Two recent retrospective studies give contradictory results, the first shows higher birth rates in the group of embryos selected according to conventional morphological criteria, the second concludes that morphokinetic analysis is superior. Morphokinetic criteria would also be more objective and reproducible. However, the use of morphokinetic parameters remains controversial in the literature.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2020
Longer than P75 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 14, 2019
CompletedFirst Posted
Study publicly available on registry
January 16, 2019
CompletedStudy Start
First participant enrolled
October 26, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2026
CompletedFebruary 20, 2026
February 1, 2026
5.3 years
January 14, 2019
February 17, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
The primary endpoint of this study will be the live birth rate by fresh embryo transfer(s).
36 months
Study Arms (2)
Conventional morphology arm (reference method)
ACTIVE COMPARATORMorphokinetic arm
EXPERIMENTALInterventions
The embryos will be observed at a fixed time and according to morphological criteria (Alpha Specialist Group in Reproductive Medicine and ESHRE, 2011). and all the films obtained will be analyzed. Embryos will be classified according to morphokinetic criteria (Ciray et al., 2014).
Eligibility Criteria
You may qualify if:
- For the couple:
- Couple whose two members are 18 years old and over,
- Couple whose two members are affiliated to a social security scheme,
- Couple whose two members read and understood the newsletter and signed the consent form for their participation in this research.
- For the conditions of realization of the ICSI attempt:
- Couple supported for a 1st or 2nd attempt at in vitro fertilization with sperm microinjection (ICSI) for male infertility,
- In vitro fertilization attempt performed with micro-injection of fresh ejaculated spermatozoa.
- For the man:
- Couple whose man has an alteration of at least one of the sperm parameters according to the WHO (WHO, 2010) for the number, concentration, vitality, mobility or morphology according to the modified David classification (Auger and Eustache, 2000).
You may not qualify if:
- For the couple:
- Couple whose wife is under 18 and over 42 and / or the male is under 18 and over 59
- Couple already included in the protocol "EMCIMO" for a previous attempt,
- Couple of which one or both members is deprived by an administrative or judicial decision or subject to a legal measure of protection of the majors (safeguard of justice or tutelage or curatorship),
- Couple where one or both members do not speak or understand French.
- For the conditions of realization of the ICSI attempt:
- \- In vitro fertilization attempt with the micro-injection of testicular spermatozoa, epididymal, previously frozen or resulting from a retrograde ejaculation.
- For the man:
- Severe oligozoospermia (\<100,000 spermatozoa / ejaculate).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
CHU CAEN
Caen, 14033, France
Chu Rouen
Rouen, 76031, France
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 14, 2019
First Posted
January 16, 2019
Study Start
October 26, 2020
Primary Completion
March 1, 2026
Study Completion
March 1, 2026
Last Updated
February 20, 2026
Record last verified: 2026-02