Clin2
NCT06566066Possibly a fitRecruiting

Thyroid hormone resistance patient registry

HypothyroidismGlobal Developmental DelayIntellectual DisabilityDystoniaMuscle HypotoniaSeizuresAllan-Herndon-Dudley SyndromeMicrocephalus

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital, Hormones & metabolism, Mental health clinical trials.

This study creates a registry for people with thyroid hormone resistance caused by specific genetic mutations. It helps doctors collect data to better understand and treat the condition.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
200 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a mutation in the SLC16A2 or THRA gene.
  • Your blood tests show an abnormal fT3/fT4 ratio.
  • You or your caregiver agree to join the study.
  • You have not withdrawn your consent or had your diagnosis changed.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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