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NCT06576830 · ClinicalTrials.gov registry record · Phase 4
Optimization of Pediatric Tonsillectomy to IMprove AnaLgesia
A Phase 4 study of Pain, Postoperative and Sleep Disordered Breathing, sponsored by Duke University.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 440
- Enrollment target
- 1
- Study location
NCT06576830 is a Phase 4 study of Pain, Postoperative and Sleep Disordered Breathing that is actively recruiting participants, run by Duke University. The registered enrollment target is 440 participants, above the 269-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (64% higher). The trial reports 1 study location across 1 state.
The verdict
NCT06576830, a Phase 4 study of Pain, Postoperative and Sleep Disordered Breathing, is actively recruiting participants, sponsored by Duke University.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 440 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare the use of short acting opioids (fentanyl/hydromorphone) with long acting opioids (methadone) for pain control following tonsillectomy surgery in children and adolescents.
Conditions Studied
Interventions
- DRUG Methadone
- DRUG Fentanyl/Hydromorphone
Study Locations (1)
North Carolina
- Duke University Medical Center - Durham
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 440 participants |
| Start Date | 2024-11-21 |
| Est. Completion | 2029-06-01 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06576830
The ClinicalTrials.gov registry entry for NCT06576830 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 440 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 269-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (64% higher). The listed sponsor is Duke University, which has 1,725 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Methadone is the first listed.
NCT06576830 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT06576830 about?
NCT06576830 is a clinical study titled "Optimization of Pediatric Tonsillectomy to IMprove AnaLgesia". The purpose of this study is to compare the use of short acting opioids (fentanyl/hydromorphone) with long acting opioids (methadone) for pain control following tonsillectomy surgery in children and adolescents.
What is the current status of trial NCT06576830?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 440 participants. The study started on 2024-11-21. Estimated completion is 2029-06-01.
What conditions does trial NCT06576830 study?
This clinical trial studies the following conditions: Pain, Postoperative, Sleep Disordered Breathing, Tonsillitis, Tonsillar Hypertrophy, Pediatric Sleep Apnea.
What interventions are being tested in trial NCT06576830?
The interventions under investigation include: Methadone (DRUG), Fentanyl/Hydromorphone (DRUG).
Who is sponsoring clinical trial NCT06576830?
This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06576830 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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