Maternal and Fetal Compatibility in Assisted Reproductive Technology (ART)-Oocyte Donor Influences Live Birth Rate

NCT ID: NCT02718105

Last Updated: 2022-08-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-01-01

Study Completion Date

2022-08-01

Brief Summary

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Has the maternal KIR haplotype an impact in pregnancy, miscarriage and live birth rates per embryo transfer in donor oocytes -ART by paternal and oocyte donor HLA-C?

Detailed Description

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The combination of maternal KIR haplotype and parental, donors HLA-C, could predict which couple can benefit for the selection of single embryo transfer (SET)/double embryo transfer (DET), or donor selection by HLA-C in ART, in order to increase the live birth rate (LBR)/cycle since HLA-C1/C1 donors are predicted to be safer and C2/C2 males or oocyte donors may be mor "dangerous" as identified by epidemiological studies

Conditions

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Infertility

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Receiver patients in donor oocyte -ART

Maternal and fetal compatibility KIR HLA-C determinations in ART -oocyte donor

KIR HLAC determinations

Intervention Type GENETIC

We will take blood samples for KIR HLA-C determinations.

Interventions

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KIR HLAC determinations

We will take blood samples for KIR HLA-C determinations.

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* BMI between 19 - 27 kg/m2
* Blastocyst embryo transfer previous.
* Normal karyotype, thrombophylic and immunological results.
* Normal clinical history, viral serology, hormonal analysis (TSH, T4, prolactin, estrogen, progesterone), spermiogram, sperm FISH and pelvic ultrasound results.

Exclusion Criteria

* Pregnancy women.
* Psychiatric disorders.
* Uterus alterations.
* Polycystic ovary syndrome
* Genetic and autoimmune diseases.
* Infectious diseases.
* Corticoid and immunosuppressant treatments previous.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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IVI Madrid

OTHER

Sponsor Role lead

Responsible Party

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Juan A Garcia-Velasco

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Juan Antonio Garcia Velasco, PhD

Role: PRINCIPAL_INVESTIGATOR

IVI Madrid

Locations

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Instituto Valenciano de Infertilidad

Madrid, , Spain

Site Status

Countries

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Spain

Other Identifiers

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1512-MAD-067-JG

Identifier Type: -

Identifier Source: org_study_id

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