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NCT00508066 · ClinicalTrials.gov registry record · Phase 4
Continuous Local Infusion of Anesthetic at the Incisional Site for Scoliosis Surgery
A Phase 4 study, sponsored by Shriners Hospitals for Children.
- Completed
- Registry status
- Phase 4
- Development phase
- 60
- Enrollment target
NCT00508066: Completed Phase 4 study, sponsored by Shriners Hospitals for Children.
NCT00508066 is a Phase 4 study that has completed, run by Shriners Hospitals for Children. The registered enrollment target is 60 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00508066, a Phase 4 study, has completed, sponsored by Shriners Hospitals for Children.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 60 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the effects of continuous local anesthetic delivery on the immediate post-op recovery of patients undergoing spinal fusion surgery for congenital or idiopathic scoliosis.
Interventions
- DRUG Bupivacaine
- DRUG Normal Saline
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2007-05 |
| Est. Completion | 2011-01 |
| Phase | Phase 4 |
What the finished NCT00508066 record still lists
NCT00508066 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 2 interventions - of which Bupivacaine is the first listed.
NCT00508066 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00508066 about?
NCT00508066 is a clinical study titled "Continuous Local Infusion of Anesthetic at the Incisional Site for Scoliosis Surgery". The purpose of this study is to evaluate the effects of continuous local anesthetic delivery on the immediate post-op recovery of patients undergoing spinal fusion surgery for congenital or idiopathic scoliosis.
What is the current status of trial NCT00508066?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2007-05. Estimated completion is 2011-01.
What interventions are being tested in trial NCT00508066?
The interventions under investigation include: Bupivacaine (DRUG), Normal Saline (DRUG).
Who is sponsoring clinical trial NCT00508066?
This trial is sponsored by Shriners Hospitals for Children, which has 40 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00508066's enrollment target sits among peer trials
60 1125th of 2000 higher than 799 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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