NL-OMON31988
Not yet recruiting
Not Applicable
Sex chromosome abnormality as co-finding when performing routine prenatal diagnostic procedures: diagnostic gain or damage? Study on the views of parents and professionals. - Routine fetal gender determination in prenatal testing: gain or damage?
niversitair Medisch Centrum Sint Radboud0 sites30 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- foetale geslachtsbepaling
- Sponsor
- niversitair Medisch Centrum Sint Radboud
- Enrollment
- 30
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Parents that have undergone an invasive prenatal diagnostic test in the last 15 years in the Nijmegen region because of maternal age or to exclude other serious chromosomal anomalies, who were faced with a fetal sex chromosomal abnormality as a co\-finding in the karyotyping procedure.
Exclusion Criteria
- •. Patients with a clear risk at a sex chromosomal abnormality, because of an earlier child with this same problem.
- •. Patients with insufficient fluency in Dutch.
Outcomes
Primary Outcomes
Not specified
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