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Recruiting NCT06523543

Ultra-early Identification of Fetal Chromosomal Characteristics From Extravillous-trophoblast Cells

Observational Pregnant Women

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Inclusion (Visit 1 - Week 7-16), Second semester of pregnancy (Visit 2 - Week 20-24), Third semester of pregnancy (Visit 3- Week 34).
Who it may be relevant to
Registry conditions: Pregnant Women. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Demonstrate the efficacy of an ultra-early, non-invasive prenatal diagnostic method adaptable to various genetic indications to detect fetal chromosomal abnormalities.

Detailed description

During pregnancy, biological screening for genetic diseases of the fetus cannot be implemented before the 11th week of amenorrhea whatever the technique used. This delay is long and distressing, particularly for people at high risk of transmission of genetic diseases. The presence of extravillous trophoblast cells to the cervix of the pregnant woman from the 7th week, accessible by a cervicovaginal smear non-invasive, represents new biological material representative of the fetal genome. This project aimed at evaluating the performance of a method for analyzing these trophoblast cells extra-villous at the start of pregnancy. The investigators want to evaluate performance analytical aspects of this method, that is to say, verifying that the genetic information resulting from these cells correspond to those of the fetus.

Interventions

  • Procedure Inclusion (Visit 1 - Week 7-16)
    Extraction of cervico-vaginal sampling
  • Diagnostic test Second semester of pregnancy (Visit 2 - Week 20-24)
    Ultrasound examination (determination of chromosomal sex)
  • Diagnostic test Third semester of pregnancy (Visit 3- Week 34)
    Ultrasound examination (determination of chromosomal sex) if this has not be done during the Visit 2 or if a new determination correcting the previous one is provided.

Primary outcome measures

  • Establish an ultra-early detection method [Time frame: Visit 2 (Week 20-24)]
Secondary outcome measures (2)
  • Evaluate the ability of the method to provide a result in the context of a progressive pregnancy [Time frame: Visit 2 (Week 20-24)]
  • Expected benefit of ultra-early cytogenetic information [Time frame: Visit 2 (Week 20-24)]

Eligibility criteria

Inclusion criteria

  • Pregnant woman
  • Singleton pregnancy
  • Pregnancy between 7 and 16 weeks of amenorrhea (WA)
  • Woman ≥ 18 years
  • Woman who has signed an informed consent
  • Woman affiliated to social security or equivalent scheme

Exclusions Criteria:

  • Person under guardianship or curatorship
  • Person placed under legal protection
  • Person unable to provide the participant with informed consent.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

France · 1 center
  • CHU de Montpellier — Montpellier

Publications

  • Bailey-Hytholt CM, Sayeed S, Kraus M, Joseph R, Shukla A, Tripathi A. A Rapid Method for Label-Free Enrichment of Rare Trophoblast Cells from Cervical Samples. Sci Rep. 2019 Aug 20;9(1):12115. doi: 10.1038/s41598-019-48346-3. PMID 31431640
  • Bolnick JM, Kilburn BA, Bajpayee S, Reddy N, Jeelani R, Crone B, Simmerman N, Singh M, Diamond MP, Armant DR. Trophoblast retrieval and isolation from the cervix (TRIC) for noninvasive prenatal screening at 5 to 20 weeks of gestation. Fertil Steril. 2014 Jul;102(1):135-142.e6. doi: 10.1016/j.fertnstert.2014.04.008. Epub 2014 May 10. PMID 24825422
  • Drewlo S, Armant DR. Quo vadis, trophoblast? Exploring the new ways of an old cell lineage. Placenta. 2017 Dec;60 Suppl 1(Suppl 1):S27-S31. doi: 10.1016/j.placenta.2017.04.021. Epub 2017 Apr 26. PMID 28483162
  • Fritz R, Kohan-Ghadr HR, Bolnick JM, Bolnick AD, Kilburn BA, Diamond MP, Drewlo S, Armant DR. Noninvasive detection of trophoblast protein signatures linked to early pregnancy loss using trophoblast retrieval and isolation from the cervix (TRIC). Fertil Steril. 2015 Aug;104(2):339-46.e4. doi: 10.1016/j.fertnstert.2015.05.010. Epub 2015 Jun 11. PMID 26051097
  • Kadam L, Jain C, Kohan-Ghadr HR, Krawetz SA, Drewlo S, Armant DR. Endocervical trophoblast for interrogating the fetal genome and assessing pregnancy health at five weeks. Eur J Med Genet. 2019 Aug;62(8):103690. doi: 10.1016/j.ejmg.2019.103690. Epub 2019 Jun 18. PMID 31226440
  • Mantzaris D, Cram DS. Potential of syncytiotrophoblasts isolated from the cervical mucus for early non-invasive prenatal diagnosis: evidence of a vanishing twin. Clin Chim Acta. 2015 Jan 1;438:309-15. doi: 10.1016/j.cca.2014.09.002. Epub 2014 Sep 8. PMID 25218787
  • Moser G, Drewlo S, Huppertz B, Armant DR. Trophoblast retrieval and isolation from the cervix: origins of cervical trophoblasts and their potential value for risk assessment of ongoing pregnancies. Hum Reprod Update. 2018 Jul 1;24(4):484-496. doi: 10.1093/humupd/dmy008. PMID 29608700
  • Pfeifer I, Benachi A, Saker A, Bonnefont JP, Mouawia H, Broncy L, Frydman R, Brival ML, Lacour B, Dachez R, Paterlini-Brechot P. Cervical trophoblasts for non-invasive single-cell genotyping and prenatal diagnosis. Placenta. 2016 Jan;37:56-60. doi: 10.1016/j.placenta.2015.11.002. Epub 2015 Nov 11. PMID 26680636

Identifiers

NCT: NCT06523543 · RECHMPL23_0417

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗