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In search of thyroid hormone receptor alpha-1 mutations in adolescents with delayed puberty

In search of thyroid hormone receptor alpha-1 mutations in adolescents with delayed puberty - TR alpha-1 mutations in adolescents with delayed puberty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33241
Enrollment
40
Registered
2009-11-30
Start date
2009-10-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

constitutional delay of puberty delayed puberty

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Diagnosis of delayed puberty of unknow origin, or defined as constitutional delay of puberty

Exclusion criteria

Exclusion criteria: Permanent forms of hypogonadotropic hypogonadism Hypergonadotropic hypogonadism Age

Design outcomes

Primary

MeasureTime frame
TRalpha-1 mutations

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)