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NCT06471348 · ClinicalTrials.gov registry record · NA
Postoperative Pain Control in AIS Using Liposomal Bupivacaine vs. 0.25% Bupivacaine With Epinephrine
A NA study of Post Operative Pain and Spinal Fusion, sponsored by Boston Children's Hospital.
- Recruiting
- Registry status
- NA
- Development phase
- 128
- Enrollment target
- 1
- Study location
NCT06471348 is a NA study of Post Operative Pain and Spinal Fusion that is actively recruiting participants, run by Boston Children's Hospital. The registered enrollment target is 128 participants, below the 234-participant average among 56 other Post Operative Pain trials with a reported enrollment target (45% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06471348, a NA study of Post Operative Pain and Spinal Fusion, is actively recruiting participants, sponsored by Boston Children's Hospital.
- RECRUITING
- Registry status
- NA
- Development phase
- 128 participants
- Enrollment target
- 1
- Study location
Study Summary
A randomized controlled trial (RCT) investigating whether the local anesthetic injection of liposomal bupivacaine during posterior spinal fusion (PSF) for AIS is more effective in reducing acute postoperative opioid consumption compared to an equal volume injection of 0.25% bupivacaine with epinephrine for patients aged 10 to 17, with 128 patients randomly assigned to one of two arms: liposomal bupivacaine or 0.25% bupivacaine with epinephrine.
Conditions Studied
Interventions
- DRUG Bupivacaine liposome injectable suspension
- DRUG Bupivacaine Hydrochloride and Epinephrine Injection
Study Locations (1)
Massachusetts
- Boston Children's Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 128 participants |
| Start Date | 2025-08-15 |
| Est. Completion | 2028-08-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06471348
The ClinicalTrials.gov registry entry for NCT06471348 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 128 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 234-participant average among 56 other Post Operative Pain trials with a reported enrollment target (45% lower). The listed sponsor is Boston Children's Hospital, which has 462 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Post Operative Pain appearing as the primary indexed condition, and to 2 interventions - of which Bupivacaine liposome injectable suspension is the first listed.
NCT06471348 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT06471348 about?
NCT06471348 is a clinical study titled "Postoperative Pain Control in AIS Using Liposomal Bupivacaine vs. 0.25% Bupivacaine With Epinephrine". A randomized controlled trial (RCT) investigating whether the local anesthetic injection of liposomal bupivacaine during posterior spinal fusion (PSF) for AIS is more effective in reducing acute postoperative opioid consumption compared to an equal volume injection of 0.25% bupivacaine with epinephr...
What is the current status of trial NCT06471348?
This trial is currently recruiting. It is a NA study. The enrollment target is 128 participants. The study started on 2025-08-15. Estimated completion is 2028-08-31.
What conditions does trial NCT06471348 study?
This clinical trial studies the following conditions: Post Operative Pain, Spinal Fusion.
What interventions are being tested in trial NCT06471348?
The interventions under investigation include: Bupivacaine liposome injectable suspension (DRUG), Bupivacaine Hydrochloride and Epinephrine Injection (DRUG).
Who is sponsoring clinical trial NCT06471348?
This trial is sponsored by Boston Children's Hospital, which has 462 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06471348 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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