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Congenital heart defects

Deep phenotyping, comprehensive genomic studies and investigations into pathomechanisms of congenital heart defects

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/06/034215
Enrollment
80
Registered
2021-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: Q289- Congenital malformation of circulatory system, unspecified

Interventions

Control Intervention1: Nil: Nil

Sponsors

Department of Biotechnology Ministry of Science and Technology Government of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: We plan to recruit 80 families affected with a congenital heart defect in aborted fetuses, neonates and children

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Molecular diagnosis and genetic counseling of participating familes with congenital heart diseaseTimepoint: The study period is for a duration of three years. However we do not have specific time point as this is an observational study. An average time to generate a report for a patient will be 6 months.—

Secondary

MeasureTime frame
Adding novel variants and/or novel genes causing congenital heart defects to the literatureTimepoint: Three years—

Countries

India

Contacts

Public ContactShalini S Nayak

Kasturba Medical College, Manipal

nayak.shalini@manipal.edu9964043502

Outcome results

None listed

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