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NCT Number: NCT05648136

Immune Profile Analysis and Biomarker Identification in Women With Repeated Implantation Failure or Unexplained Recurrent Spontaneous Miscarriage

Implantation is a determining step in human reproduction which requires the transition from a pro-inflammatory state to an anti-inflammatory state allowing the implantation of a competent embryo within a receptive endometrium, and then the maternal immunotolerance towards the alloantigenic fetus. Repeat implantation failures (RIFs), that refers to the fail to achieve a clinical pregnancy after the transfer of at least 3-4 good quality embryos or two blastocysts, and unexplained recurrent spontaneous miscarriage (RM) (≥2-3) could be related in some patients to immune imbalances characterized by an excessive and prolonged inflammatory response and/or a defect of anti-inflammatory regulation. In this context, several therapies have been evaluated in patients with RIFs or RMs in order to restore the immune balance, with heterogeneous results. No serum biomarker assay has been routinely approved to identify patients with immune imbalances that may explain repeated pregnancy failures and to predict the success of the subsequent IVF/ICSI cycle. The immunological analysis on peripheral blood will be based on the determination of the proportions of immune subpopulations (e.g. CD4+ et CD8+, TH1, TH2, TH17, Treg, ILC 1, ILC2, and ILC3) on the one hand and the circulating level of plasma cytokines on the other hand.

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Key information

Conditions

Repeated Embryo Implantation Failure Abortion, Habitual Abortion, Spontaneous Female Urogenital Diseases and Pregnancy Complications Immune System Pregnancy Complications Recurrent Miscarriage Urogenital Diseases

Age range

18 year–39 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Centre Hospitalier Universitaire d'Amiens

Amiens, Picardie, 80000, France

Location status: Recruiting

Location contact

Amandine Dernoncourt, DR

CONTACT

[email protected]

03. 22. 66. 82. 30

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • For patients :
  • Women aged 18 to 39 years
  • women with a history of RIF or unexplained RM
  • women with a negative diagnostic work-up (including pelvic ultrasound and hysteroscopy, parental karyotype, thyroid function test, and anti-thyroid and anti-phospholipid antibodies)
  • women with a basal FSH level <10IU/l and AMH level >1.5ng/ml
  • women with a regular menstrual cycle of 30+/-5 days
  • women receiving a new cycle of in vitro fertilization (IVF) +/- intracytoplasmic sperm injection (ICSI) for patients in the RIF group or a first cycle of IVF +/-ICSI for patients in the RM group
  • women received written and oral information and signed an informed consent

For control groups:

  • Controls recruited in the Obstetrics and Gynecology Department with at least one live birth after a spontaneous pregnancy (with a time to conception of less than 12 months for each pregnancy) Voluntary oocyte donors recruited within the CECOS de Picardie (having presented at least one live birth with a delay necessary to conceive of less than 12 months)
  • Controls recruited in the Reproductive Medicine and Biology Department having presented at least one live birth (spontaneous with a delay to conceive of less than 12 months for each pregnancy or after one or two MPA procedures) and benefiting from an IVF+/-ICSI procedure for secondary infertility
  • Controls recruited in the department of Medicine and Reproductive Biology with a normal infertility assessment and benefiting from an IVF procedure with ICSI on male indication.

Exclusion criteria

  • Ongoing pelvic and/or systemic infection
  • Chronic infectious endometritis
  • Active neoplasia
  • Autoimmune and autoinflammatory disease
  • Celiac disease
  • Thrombophilia (including positive anti-phospholipid antibodies)
  • Endocrine pathology (including dysthyroidism and diabetes)
  • Endometriosis
  • Polycystic ovary syndrome and ovulatory disorders
  • Premature ovarian failure
  • IVF by oocyte donation
  • Tubal obstructions or lesions, uterine and cervical anomalies
  • Partners with extreme oligoastheno-spermia and/or sperm DNA fragmentation >30
  • Sperm donations
  • Patients unable to give informed consent

Treatment and study plan

Blood sample

Biological

Blood sampling by venipuncture will be performed :

  • for patients and controls: between the 20th and 24th day of the menstrual cycle (implantation window) preceding the following IVF+/-ICSI cycle
  • for patients receiving an endometrial biopsy: on the same day as the endometrial biopsy
  • for patients and controls receiving follicular stimulation for ovarian puncture: the day of the oocyte puncture
  • for patients and controls undergoing embryo transfer: on the day of embryo implantation

Primary outcomes

  1. Variation of the proportion of CD4+ subpopulations between both patient groups

    Time frame: 18 months

  2. Variation of the proportion of CD8+ subpopulations between both patient groups

    Time frame: 18 months

  3. Variation of the proportion of TH1 subpopulations between both patient groups

    Time frame: 18 months

  4. Variation of the proportion of TH2 subpopulations between both patient groups

    Time frame: 18 months

  5. Variation of the proportion of TH17 subpopulations between both patient groups

    Time frame: 18 months

  6. Variation of the proportion of Treg subpopulations between both patient groups

    Time frame: 18 months

  7. Variation of the proportion of ILC 1 subpopulations between both patient groups

    Time frame: 18 months

  8. Variation of the proportion of ILC 2 subpopulations between both patient groups

    Time frame: 18 months

  9. Variation of the proportion of ILC 3 subpopulations between both patient groups

    Time frame: 18 months

  10. Variation of the proportion of TNFα concentrations between both patient groups

    Time frame: 18 months

  11. Variation of the proportion of IFN gamma concentrations between both patient groups

    Time frame: 18 months

  12. Variation of the proportion of TGF-β concentrations between both patient groups

    Time frame: 18 months

  13. Variation of the proportion of IL-10 concentrations between both patient groups

    Time frame: 18 months

  14. Variation of the proportion of IL-17 concentrations between both patient groups

    Time frame: 18 months

Study contacts

Contact information is provided by the study sponsor or research team.

Amandine Dernoncourt, DR

CONTACT

[email protected]

03. 22. 66. 82. 30

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire, Amiens

Other

Registry information

Acronym: ERIM

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Dec 13, 2022
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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