BPL: Biochemical Pregnancy Loss. A Multicenter Retrospective Study

Sponsor
IVI Vigo (Other)
Overall Status
Completed
CT.gov ID
NCT04549909
Collaborator
Instituto Valenciano de Infertilidad, IVI VALENCIA (Other), IVI Madrid (Other), Fundación IVI (Other)
20,000
1
11.1
1806.4

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: collect retrospectively data

Detailed Description

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.

Study Design

Study Type:
Observational
Actual Enrollment :
20000 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Is Biochemical Pregnancy Loss Associated to Embryo or Endometrium? A Multicenter Retrospective Study
Actual Study Start Date :
Feb 12, 2019
Actual Primary Completion Date :
Jan 15, 2020
Actual Study Completion Date :
Jan 15, 2020

Arms and Interventions

Arm Intervention/Treatment
preimplantation genetic testing for aneuploidy (PGT-A) Group

Patients who have undergone preimplantation genetic testing for aneuploidy (PGT-A) (transfer of own frozen embryo)

Other: collect retrospectively data
Analyse the incidence of BPL in these populations

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)

Other: collect retrospectively data
Analyse the incidence of BPL in these populations

CONTROL OWN (CO) Group

Control group of FET from own oocytes (without ERA or PGT-A)

Other: collect retrospectively data
Analyse the incidence of BPL in these populations

CONTROL DONATED(CD) Group

Control group of FET from donated oocytes (without ERA or PGT-A)

Other: collect retrospectively data
Analyse the incidence of BPL in these populations

Outcome Measures

Primary Outcome Measures

  1. Biochemical pregnancy loss (BPL) [Since 2013 to april 2019]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 44 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Patients with the following selection criteria:
  • IVF/ICSI patients aged between 18 and 44

  • BMI 18-30 kg/m2

  • Frozen embryo transfer from own oocytes after PGT-A

  • Frozen embryo transfer with ERA test (from own or donated oocytes)

  • Frozen embryo transfer (from own or donated oocytes)

  • Single embryo transfer (SET) in all cycles

  • Patients without uterine malformations

  • Patients without recurrent miscarriage (≥ 3)

  • Patients with adequate endometrial thickness (> 7mm)

  • Patients without thyroid autoimmunity

  • Patients without thrombophilia

  • Exclude cycles with exclusively PGT-M

  • Exclude FET in ovarian stimulated cycles

Exclusion Criteria:

Exclude cycles with exclusively PGT-M Exclude FET in ovarian stimulated cycles

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Contacts and Locations

Locations

Site City State Country Postal Code
1 IVI Vigo Vigo Pontevedra Spain 36203

Sponsors and Collaborators

  • IVI Vigo
  • Instituto Valenciano de Infertilidad, IVI VALENCIA
  • IVI Madrid
  • Fundación IVI

Investigators

  • Principal Investigator: Elkin DR Muñoz, MD, IVI Vigo

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
IVI Vigo
ClinicalTrials.gov Identifier:
NCT04549909
Other Study ID Numbers:
  • 1902-VGO-019-EM
First Posted:
Sep 16, 2020
Last Update Posted:
Sep 23, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by IVI Vigo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 23, 2020