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NCT02320669 · ClinicalTrials.gov registry record · Phase 3

Phase 3 Triiodothyronine Supplementation for Infants After Cardiopulmonary Bypass

A Phase 3 study, sponsored by Seattle Children's Hospital.

Completed
Registry status
Phase 3
Development phase
220
Enrollment target

NCT02320669: Completed Phase 3 study, sponsored by Seattle Children's Hospital.

NCT02320669 is a Phase 3 study that has completed, run by Seattle Children's Hospital. The registered enrollment target is 220 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02320669, a Phase 3 study, has completed, sponsored by Seattle Children's Hospital.

COMPLETED
Registry status
Phase 3
Development phase
220 participants
Enrollment target

Study Summary

This is a study to determine the safety and efficacy of liothyronine sodium/triiodothyronine (Triostat), a synthetic thyroid hormone, when given to infants with congenital heart disease during cardiopulmonary bypass surgery. Funding Source - FDA OOPD.

Primary Outcome

time on mechanical ventilation after aortic cross clamp removal

Interventions

  • DRUG Placebo
  • DRUG Triostat

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2014-11
Est. Completion 2019-10
Phase Phase 3
Seattle Children's Hospital

168 total trials

What the finished NCT02320669 record still lists

NCT02320669 is an interventional study that assigns participants to a tested intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02320669 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02320669 about?

NCT02320669 is a clinical study titled "Phase 3 Triiodothyronine Supplementation for Infants After Cardiopulmonary Bypass". This is a study to determine the safety and efficacy of liothyronine sodium/triiodothyronine (Triostat), a synthetic thyroid hormone, when given to infants with congenital heart disease during cardiopulmonary bypass surgery. Funding Source - FDA OOPD.

What is the current status of trial NCT02320669?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 220 participants. The study started on 2014-11. Estimated completion is 2019-10.

What interventions are being tested in trial NCT02320669?

The interventions under investigation include: Placebo (DRUG), Triostat (DRUG).

Who is sponsoring clinical trial NCT02320669?

This trial is sponsored by Seattle Children's Hospital, which has 168 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02320669's enrollment target sits among peer trials

220 1318th of 2000 higher than 672 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02320669, the US trial registry maintained by the National Library of Medicine. NCT02320669 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.