Study Results
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Basic Information
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TERMINATED
NA
368 participants
INTERVENTIONAL
2018-05-28
2022-02-22
Brief Summary
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The ERA test (Endometrial Receptivity Analysis) evaluates the transcriptomic endometrial profile to determine if the patient's uterus is receptive when the embryo is transferred during an In Vitro Fertilization (IVF) process, and identifies the personalized WOI of the patient. This process is called Personalized Embryo Transfer (pET).
The Preimplantation Genetic Test of Aneuploidies or PGT-A (Preimplantation Genetic Testing for Aneuploidy), is currently carried out using Next Generation Sequencing (NGS) and serves to identify chromosomally normal embryos prior to their transfer in an IVF treatment. Aneuploidies are rarely compatible with life or can cause congenital diseases. So, the identification of chromosomally normal embryos, improves the success of reproduction in cases in which infertility is caused by such aneuploidies.
Therefore, the aim of this study is to determine, in a randomized and prospective way, the clinical benefit of adding the ERA test to the embryonic aneuploidies test for patients with a PGT-A indication.
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Detailed Description
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The PGT-A is an important genetic test that was developed to select embryos during IVF treatment and avoid embryonic chromosomal abnormalities that lead to miscarriage or life born with chromosomal diseases. Embryonic aneuploidy is linked to maternal age. The most common consequences are implantation failure, miscarriage or life born with multiple congenital anomalies. The transfer of euploid embryos (chromosomally normal) diagnosed by PGT-A has shown an increase in implantation rates.
Morphology is the most traditional and routine method of embryo selection being used. However, it is difficult to distinguish normal and abnormal embryos by observing their morphology under a microscope. Therefore, morphological analysis should not be the only technique used to decide which embryo should be transferred. Application of NGS in PGT-A cycles demonstrates that this methodology is reliable, allowing identification and transfer of euploid embryos resulting in ongoing pregnancies. However, despite the transfer of morphologically normal euploid embryos, it is not always possible to acquire optimal results in Assisted Reproductive Techniques (ART).
On the other hand, the endometrial gene expression profile allows the diagnosis of the endometrium receptivity status. This is carried out by a molecular tool developed and patented by Igenomix (PCT/ES2009/00386). The ERA test is a customized expression microarray that identifies the transcriptomic expression profile signature of the personalized Window of Implantation (pWOI). A bioinformatic predictor determines the moment of maximum receptivity, indicating the best time to perform a pET.
If the result of the ERA test is "Receptive", the WOI and the moment of taking the biopsy overlap. Nevertheless, if the result is "Pre-Receptive", the optimal implantation window is expected to be after the moment in which the biopsy is taken, and if the diagnosis is "Post-Receptive", the optimal window of implantation is prior to the biopsy. In a subsequent cycle, a pET will be performed according to the ERA test results.
Recently, it has been conducted a pilot study in patients with previous implantation failures with PGT-A and euploid embryo transfer (ET). The results of the ERA test have shown that a high percentage of these patients have been diagnosed as Non-receptive (90%). This percentage is higher than the expected in the normal population (12-20%) or in the Repeated Implantation Failure (RIF) patients without PGT-A (25-30%). Once the pET was performed according to the results of the ERA test, the gestation rate was 55.55%.
So, the objective of the present study is to validate these preliminary results in a prospective, multi-center, randomized and controlled study to demonstrate the value of the endometrial factor and the improvement of the results obtained in patients with PGT-A indication. If confirmed, it would be recommended the ERA test for all ART patients, not only for those with PGT-A, demonstrating the significance in searching for the pWOI to improve reproductive outcomes.
Considering a maximum drop-out rate of 30%, a total of 750 participants are expected to be included. According to the approved protocol, an interim analysis is planned at 50% of the total enrolment.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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PGT-A without ERA
Patients with PGT-A indication and ET in a Hormone Replacement Therapy (HRT cycle) according to the usual clinical practice (day 5 of progesterone supplementation: P+5/120h).
PGT-A
PGT-A will be carried out following the usual clinical practice. Trophectoderm biopsy samples from blastocysts are analyzed by NGS to screen for numerical chromosomal abnormalities.
PGT-A and test ERA
Patients with PGT-A indication and pET in HRT cycle following the ERA test indication (when the WOI is confirmed as "Receptive").
PGT-A
PGT-A will be carried out following the usual clinical practice. Trophectoderm biopsy samples from blastocysts are analyzed by NGS to screen for numerical chromosomal abnormalities.
ERA Test
The ERA test requires an endometrial biopsy and will determine if the endometrium is receptive or not by analysing the expression levels of 236 genes involved in endometrial receptivity, to assess the optimal time to place an embryo into the uterus and promote a successful implantation and pregnancy.
Interventions
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PGT-A
PGT-A will be carried out following the usual clinical practice. Trophectoderm biopsy samples from blastocysts are analyzed by NGS to screen for numerical chromosomal abnormalities.
ERA Test
The ERA test requires an endometrial biopsy and will determine if the endometrium is receptive or not by analysing the expression levels of 236 genes involved in endometrial receptivity, to assess the optimal time to place an embryo into the uterus and promote a successful implantation and pregnancy.
Eligibility Criteria
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Inclusion Criteria
* Patients who already have frozen euploid blastocysts (day 5/6 development) analysed by PGT-A.
* Patients with embryos obtained from their own oocytes fertilized by Intracytoplasmic Sperm Injection (ICSI) or In vitro fertilization (IVF).
* Patients with an expected embryo transfer of one or two embryos (Single ET or Double ET) in a HRT cycle.
* Body Mass Index: 18,5-30 Kg/m2.
Exclusion Criteria
* Any illness or medical condition that is unstable or which, according to medical criteria, may put at risk the patient's safety and her compliance in the study.
FEMALE
No
Sponsors
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Igenomix
INDUSTRY
Responsible Party
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Principal Investigators
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Carlos Simón, MD PhD
Role: STUDY_CHAIR
Igenomix
Locations
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Ovation Fertility Newport Beach
Newport Beach, California, United States
Fertility Centers of New England
Reading, Massachusetts, United States
Pregna Medicina Reproductiva
CABA, , Argentina
Vida Bem Vinda
São Paulo, , Brazil
Olive Fertility Center
Vancouver, , Canada
Shady Grove Fertility Chile
Vitacura, , Chile
Georgian- American Center for Reproductive Medicine ReproART
Tbilisi, , Georgia
OASIS centre for reproductive medicine
Banjara Hills, Hyderabad, India
Mother And Child Hospital
Defence Colony, National Capital Territory of Delhi, India
NASCERE
Mexico City, Mexico City, Mexico
Milenium Centro Médico y de Bienestar de Alcobendas - Sanitas
Alcobendas, Madrid, Spain
Instituto Extremeño de Reproducción Asistida S.L. (IERA)
Badajoz, , Spain
Taiwan IVF Group
Zhubei, , Taiwan
Bahceci Group
Istanbul, , Turkey (Türkiye)
Vinmec Time City International Hospital
Hà Nội, , Vietnam
Countries
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Other Identifiers
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IGX1-P&E-DV-17-08
Identifier Type: -
Identifier Source: org_study_id
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