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Study identifier: NCT06724224 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Comparison of Levothyroxine Formulations in the Treatment of Congenital Hypothyroidism

Condition: Congenital Hypothyroidism  ·  Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna

PhaseN/A
Planned participants120
Who can joinAll sexes, N/A to 11 Years
Healthy volunteersNo

About this study

Observational, retrospective, prospective, pharmacological, single-centre, non-profit study. The aim is to evaluate, in newborns diagnosed with Congenital Hypothyroidism, the medium- and long-term efficacy and safety of the new formulation of levothyroxine in oral solution, compared to the liquid drop formulation and the tablet formulation. The study will involve male and female patients referred to the Neonatal Screening Centre at the Centre for Endocrine-Metabolic Diseases of the Paediatrics Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna Policlinico di S. Orsola, Italy, who tested positive for Congenital Hypothyroidism.

This description comes directly from the study's public registry record.

Talk to the study team

Rita Ortolano, MD  ·  0512144816  ·  rita.ortolano@aosp.bo.it

Always discuss trial participation with your own doctor first.

Locations (1)

IRCCS Azienda Ospedaliero-Universitaria di BolognaBologna, Bologna, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06724224