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NCT01244126 · ClinicalTrials.gov registry record · Phase 4
Postoperative Effects of Intranasal Fentanyl, IV and IM Morphine in Children Undergoing Myringotomy
A Phase 4 study, sponsored by Baylor College of Medicine.
- Completed
- Registry status
- Phase 4
- Development phase
- 171
- Enrollment target
NCT01244126: Completed Phase 4 study, sponsored by Baylor College of Medicine.
NCT01244126 is a Phase 4 study that has completed, run by Baylor College of Medicine. The registered enrollment target is 171 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01244126, a Phase 4 study, has completed, sponsored by Baylor College of Medicine.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 171 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the difference in effect of three clinically common methods of providing pain medication during surgery for ventilating tubes placed for recurring ear infections.The methods are fentanyl dripped in the nose, morphine injected in a muscle, and morphine injected in a vein.
Primary Outcome
FLACC assigns 0-2 points for each of 5 categories (face, legs, activity, cry, consolability)and sums these points to give a total score where high scores indicate worse pain (Paediatr Anaesth 2006; 16: 258-65)
Interventions
- DRUG Intranasal fentanyl
- DRUG IV morphine
- DRUG morphine IM
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 171 participants |
| Start Date | 2008-05 |
| Est. Completion | 2011-05 |
| Phase | Phase 4 |
What the finished NCT01244126 record still lists
NCT01244126 is an interventional study that assigns participants to a tested intervention. The registered 171 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 3 interventions - of which Intranasal fentanyl is the first listed.
NCT01244126 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01244126 about?
NCT01244126 is a clinical study titled "Postoperative Effects of Intranasal Fentanyl, IV and IM Morphine in Children Undergoing Myringotomy". The purpose of this study is to compare the difference in effect of three clinically common methods of providing pain medication during surgery for ventilating tubes placed for recurring ear infections.The methods are fentanyl dripped in the nose, morphine injected in a muscle, and morphine injected...
What is the current status of trial NCT01244126?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 171 participants. The study started on 2008-05. Estimated completion is 2011-05.
What interventions are being tested in trial NCT01244126?
The interventions under investigation include: Intranasal fentanyl (DRUG), IV morphine (DRUG), morphine IM (DRUG).
Who is sponsoring clinical trial NCT01244126?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01244126's enrollment target sits among peer trials
171 484th of 2000 higher than 1,517 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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