Researchers study digoxin dosing in infants with rare heart condition

NCT ID NCT06613477

First seen Nov 01, 2025 · Last updated Jun 23, 2026 · Updated 34 times

Summary

This study looks at how the heart medication digoxin is processed in infants born with single ventricle heart disease. Researchers will collect blood samples during routine care to measure drug levels. The goal is to better understand dosing, but the study does not change the infant's treatment plan. About 20 infants under 6 months old will participate.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Duke University Medical Center

    RECRUITING

    Durham, North Carolina, 27701, United States

    Contact Email: •••••@•••••

  • Medical University of South Carolina

    NOT_YET_RECRUITING

    Charleston, South Carolina, 29425, United States

    Contact Email: •••••@•••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

digoxin (Lanoxin)

What this could lead to

If successful, this could lead to more precise digoxin dosing for infants with single ventricle heart disease, potentially improving heart function and reducing side effects.

What could go wrong

This is an early-phase study with only 20 infants, so results may not apply to all patients. The study does not test whether digoxin improves outcomes, only how it is processed.

Conditions

The condition(s) this trial relates to.

Infant, Newborn, Diseases Infant, Premature, Diseases perinatal disease univentricular heart

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.