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| Name | Class |
|---|---|
| Instituto Valenciano de Infertilidad, IVI VALENCIA | OTHER |
| IVI Madrid | OTHER |
| Fundación IVI | OTHER |
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Biochemical pregnancy loss (BPL) is a very frequent issue in human reproduction. After the implantation of the embryo, hCG disappears very soon from the maternal bloodstream and no evidence of a clinical pregnancy is seen. Different studies showed that factors such as age, oocyte and embryo quality, and endometrium receptivity may have something to do with the occurrence of biochemical pregnancy loss post assisted reproduction treatment.
The main aim of this study is to evaluate the incidence of biochemical pregnancy loss (BPL) in three different cohort populations; patients undergoing frozen embryo transfer (FET) from own oocytes after preimplantation genetic testing for aneuploidy (PGT-A), patients undergoing FET from own and donated oocytes and with endometrial receptivity array (ERA), and patients undergoing FET from own or donated oocytes (without PGTA or ERA test).
We will analyse the incidence of BPL in these populations and try to determine the role of the euploid status embryo in the first group, the endometrium in the second group and the third one as control group. We are waiting to find the value of both players in the origin of BPL.
Human embryo implantation is a poorly understood process. Once the embryo implants in the endometrium, it starts to secrete hCG that can be measured in the maternal blood as early as 9 days after implantation. Only a minimal number of pregnancies get to newborn, and the majority are lost before reach the first trimester (Larsen et al., 2013).
We are looking for the role of the embryo after controlling its chromosomal ploidy, and the endometrium after controlling its transcriptomic expression. We will also use a no exposed group to the controlled euploid embryo factor neither endometrial factor that is the oocyte donation group. This analysis expects to provide more information about the key role of embryo or endometrium in BPL.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| preimplantation genetic testing for aneuploidy (PGT-A) Group | Patients who have undergone preimplantation genetic testing for aneuploidy (PGT-A) (transfer of own frozen embryo) |
| |
| endometrial receptivity array (ERA) Group | Patients who have undergone frozen embryo transfer (FET) with endometrial receptivity array (ERA) test (embryos from own or donated oocytes) |
| |
| CONTROL OWN (CO) Group | Control group of FET from own oocytes (without ERA or PGT-A) |
| |
| CONTROL DONATED(CD) Group | Control group of FET from donated oocytes (without ERA or PGT-A) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| collect retrospectively data | Other | Analyse the incidence of BPL in these populations |
|
| Measure | Description | Time Frame |
|---|---|---|
| Biochemical pregnancy loss (BPL) | when the maternal serum levels of β-hCG are higher than 10 UI/L, but in the transvaginal ultrasound is not possible to appreciate any gestational structure (dichotomous qualitative variable: yes/no). This variable is considered as the fraction between patients whose β-hCG is higher than 10 UI/L, without clinically recognized pregnancy, by number of pregnant patients. | Since 2013 to april 2019 |
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Inclusion Criteria:
Patients with the following selection criteria:
Exclusion Criteria:
Exclude cycles with exclusively PGT-M Exclude FET in ovarian stimulated cycles
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Infertile patients who come to participating centres for assisted reproduction treatments. Patients will be divided into 4 groups according to the treatment carried out: PGT-A, ERA, FET from own oocytes (CO) or FET from donated oocytes (CD).
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| Name | Affiliation | Role |
|---|---|---|
| Elkin DR Muñoz, MD | IVI Vigo | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| IVI Vigo | Vigo | Pontevedra | 36203 | Spain |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 20619403 | Result | Diaz-Gimeno P, Horcajadas JA, Martinez-Conejero JA, Esteban FJ, Alama P, Pellicer A, Simon C. A genomic diagnostic tool for human endometrial receptivity based on the transcriptomic signature. Fertil Steril. 2011 Jan;95(1):50-60, 60.e1-15. doi: 10.1016/j.fertnstert.2010.04.063. Epub 2010 Jul 8. | |
| 38775331 | Derived |
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| ID | Term |
|---|---|
| D000022 | Abortion, Spontaneous |
| ID | Term |
|---|---|
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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| Munoz E, Taboas E, Alvarez M, Gil E, Perez A, Portela S, Martinez-Chapela M, Saucedo E, Garrido N. Is biochemical pregnancy loss associated with embryo or endometrium? A retrospective cohort study in frozen single embryo transfer of own and donated oocytes. Hum Reprod. 2024 May 22:deae106. doi: 10.1093/humrep/deae106. Online ahead of print. |