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NCT00515281 · ClinicalTrials.gov registry record · Phase 2

Inhaled Nitric Oxide and Neuroprotection in Premature Infants

A Phase 2 study, sponsored by University of Chicago.

Terminated
Registry status
Phase 2
Development phase
273
Enrollment target

NCT00515281: Clinical Trial Phase 2 study, sponsored by University of Chicago.

NCT00515281 is a Phase 2 study that was terminated before completion, run by University of Chicago. The registered enrollment target is 273 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (105% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00515281, a Phase 2 study, was terminated before completion, sponsored by University of Chicago.

TERMINATED
Registry status
Phase 2
Development phase
273 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether inhaled nitric oxide improves the neurological outcome for premature infants.

Interventions

  • DRUG inhaled nitric oxide
  • DRUG oxygen

Trial Details

FieldValue
Enrollment Target 273 participants
Start Date 2008-05
Est. Completion 2023-11-28
Phase Phase 2
University of Chicago

796 total trials

Why NCT00515281 stopped before completion

NCT00515281 is an interventional study that assigns participants to a tested intervention. The registered 273 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (105% higher).

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

NCT00515281 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00515281 about?

NCT00515281 is a clinical study titled "Inhaled Nitric Oxide and Neuroprotection in Premature Infants". The purpose of this study is to determine whether inhaled nitric oxide improves the neurological outcome for premature infants.

What is the current status of trial NCT00515281?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 273 participants. The study started on 2008-05. Estimated completion is 2023-11-28.

What interventions are being tested in trial NCT00515281?

The interventions under investigation include: inhaled nitric oxide (DRUG), oxygen (DRUG).

Who is sponsoring clinical trial NCT00515281?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00515281's enrollment target sits among peer trials

273 204th of 2000 higher than 1,797 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00515281, the US trial registry maintained by the National Library of Medicine. NCT00515281 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.