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NCT00152542 · ClinicalTrials.gov registry record · Phase 3
Follow-up at School-age of Children Who Participated in the Efficacy Study of Nitric Oxide for Premature Infants
A Phase 3 study, sponsored by University of Chicago.
- Completed
- Registry status
- Phase 3
- Development phase
- 160
- Enrollment target
NCT00152542: Completed Phase 3 study, sponsored by University of Chicago.
NCT00152542 is a Phase 3 study that has completed, run by University of Chicago. The registered enrollment target is 160 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00152542, a Phase 3 study, has completed, sponsored by University of Chicago.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 160 participants
- Enrollment target
Study Summary
Our previous data demonstrated that premature infants treated with inhaled nitric oxide at birth had improved neurodevelopmental outcomes at two years corrected age. We now wish to determine whether this benefit continues through school age.
Interventions
- DRUG Placebo
- DRUG Inhaled nitric oxide
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2005-05 |
| Est. Completion | 2006-09 |
| Phase | Phase 3 |
What the finished NCT00152542 record still lists
NCT00152542 is an interventional study that assigns participants to a tested intervention. The registered 160 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 (79% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00152542 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00152542 about?
NCT00152542 is a clinical study titled "Follow-up at School-age of Children Who Participated in the Efficacy Study of Nitric Oxide for Premature Infants". Our previous data demonstrated that premature infants treated with inhaled nitric oxide at birth had improved neurodevelopmental outcomes at two years corrected age. We now wish to determine whether this benefit continues through school age.
What is the current status of trial NCT00152542?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 160 participants. The study started on 2005-05. Estimated completion is 2006-09.
What interventions are being tested in trial NCT00152542?
The interventions under investigation include: Placebo (DRUG), Inhaled nitric oxide (DRUG).
Who is sponsoring clinical trial NCT00152542?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00152542's enrollment target sits among peer trials
160 1479th of 2000 higher than 500 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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