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Correlation between genotype, phenotype and treatment effect of congenital hypothyroidism

Correlation between genotype, phenotype and treatment effect of congenital hypothyroidism

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102155
Enrollment
Unknown
Registered
2025-05-09
Start date
2024-08-21
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

congenital hypothyroidism

Interventions

Grouping by congenital hypothyroidism-related gene mutation results:None

Sponsors

Fujian Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with congenital hypothyroidism who visited our outpatient clinic from January 2021 to December 2024.

Exclusion criteria

Exclusion criteria: Patients with central hypothyroidism and other systemic underlying diseases were excluded.

Design outcomes

Primary

MeasureTime frame
Whole-exome genome;Thyroid ultrasound;—

Secondary

MeasureTime frame
Levothyroxine dosage;—

Countries

China

Contacts

Public ContactGao Jiaying

Fujian Children's Hospital

gphoebe@163.com+86 183 2196 2429

Outcome results

None listed

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