Skip to content

Application of whole exon sequencing in fetuses with abnormal ultrasound structures

Application of whole exon sequencing in fetuses with abnormal ultrasound structures

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025766
Enrollment
Unknown
Registered
2019-09-07
Start date
2019-09-01
Completion date
Unknown
Last updated
2019-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abnormal fetal ultrasound structure

Interventions

Nervous system malformation, skeletal malformation, digestive system malformation, cardiovascular system, urinary system, craniofacial malformation and control group:None

Sponsors

Wuhan Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Fetal structural malformation was detected in prenatal ultrasound examination and/or magnetic resonance imaging in our hospital, or was referred to our hospital for ultrasound examination and/or magnetic resonance imaging to confirm the diagnosis.Abnormalities include structural deformity, translucent thickness of neck >=3.5mm and cystic edema.

Exclusion criteria

Exclusion criteria: Isolated ultrasound soft markers, such as choroid plexus cyst, echogenic lesions in the heart or intestine, thickened neck folds, lack of nasal bone, single umbilical artery, or persistent right umbilical vein. Fetal samples will be collected using chorionic villus sampling, amniocentesis, and umbilical cord biopsy, depending on gestational age at the time of invasive prenatal testing.

Design outcomes

Primary

MeasureTime frame
CMA, WES;

Countries

China

Contacts

Public ContactHe XueLian

Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology

18971455173@189.cn+86 18971455713

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026