Paternal Age and Fetal Aneuploidy

Sponsor
Clinique Ovo (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT05981521
Collaborator
(none)
30,000
1
12
2494.9

Study Details

Study Description

Brief Summary

Trisomy 21, commonly known as down syndrome, is the most common chromosomal abnormality in humans. Advanced maternal age (AMA) is a well-recognized risk factor for trisomy 21, with the risk increasing significantly beyond the age of 35. Research on the effects of paternal age on the prenatal risk of trisomy 21 is lacking, with inconsistent findings in the literature.

The Harmony® prenatal test is an Non-Invasive Prenatal Testing (NIPT) that screens maternal blood for chromosomal abnormalities in the Cell-Free Fetal DNA (cfDNA). The harmony® prenatal test can detect conditions such as trisomy 13, 18, and 21, as well as sex chromosome abnormalities.

The Optimo test is a prenatal screening test that screens for trisomies 13, 18 and 21 in the developing fetus using extended biochemical screening in maternal. The Optimo test has shown high sensitivity and specificity in detecting trisomy 21.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Optimo prenatal screening test

Study Design

Study Type:
Observational
Anticipated Enrollment :
30000 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Exploring the Association Between Paternal Age and Trisomy 21 Screening Results.
Actual Study Start Date :
Jul 31, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Jul 31, 2024

Outcome Measures

Primary Outcome Measures

  1. Trisomy 21 screening results [3 to 5 days]

    On the day of the Optimo screening test, a questionnaire concerning clinical data (maternal and paternal age, ethnicity, weight, smoking status, pregnancy history) is completed. Blood test and nuchal transparency are done on that day. Results from serum analysis and nuchal transparency are combined to assess the risk of trisomy 21. Association between paternal age and trisomy 21 screening results will be assessed afterwards

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Pregnant women aged 18 years or older (at the time of trisomy 18 and 21 screening) and who were able to complete the questionnaire in either French or English

  • Pregnant women who completed the entire trisomy 21 screening process at clinique ovo were included

Exclusion Criteria:
  • Patients who did not indicate the male partner/donor's age were excluded

  • Patients who did not complete or sign the clinical information form

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinique Ovo Montréal Quebec Canada H4P 2S4

Sponsors and Collaborators

  • Clinique Ovo

Investigators

  • Principal Investigator: Jacques I Kadoch, MD, clinique ovo R&D department

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Clinique Ovo
ClinicalTrials.gov Identifier:
NCT05981521
Other Study ID Numbers:
  • 3321
First Posted:
Aug 8, 2023
Last Update Posted:
Aug 9, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2023