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NCT01054027 · ClinicalTrials.gov registry record · NA
Study on Effective Mydriasis in Premature Infants
A NA study, sponsored by Georgetown University.
- Completed
- Registry status
- NA
- Development phase
- 15
- Enrollment target
NCT01054027: Completed NA study, sponsored by Georgetown University.
NCT01054027 is a NA study that has completed, run by Georgetown University. The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01054027, a NA study, has completed, sponsored by Georgetown University.
- COMPLETED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the dilating effect of 0, 1, 2 or 3 drops of mydriatic (pupil dilating) in premature infants undergoing routine retinal (eye) screening exams for Retinopathy of Prematurity (ROP).
Interventions
- DRUG 1% phenylephrine and 0.2% cyclopentolate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2007-03 |
| Est. Completion | 2008-03 |
| Phase | NA |
What the finished NCT01054027 record still lists
NCT01054027 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which 1% phenylephrine and 0.2% cyclopentolate is the first listed.
NCT01054027 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01054027 about?
NCT01054027 is a clinical study titled "Study on Effective Mydriasis in Premature Infants". The purpose of this study is to compare the dilating effect of 0, 1, 2 or 3 drops of mydriatic (pupil dilating) in premature infants undergoing routine retinal (eye) screening exams for Retinopathy of Prematurity (ROP).
What is the current status of trial NCT01054027?
This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2007-03. Estimated completion is 2008-03.
What interventions are being tested in trial NCT01054027?
The interventions under investigation include: 1% phenylephrine and 0.2% cyclopentolate (DRUG).
Who is sponsoring clinical trial NCT01054027?
This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01054027's enrollment target sits among peer trials
15 1881st of 2000 higher than 92 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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