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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 is a Phase 4 study that has completed, run by Shriners Hospitals for Children. The registered enrollment target is 60 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00508066
The ClinicalTrials.gov registry entry for NCT00508066 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Shriners Hospitals for Children, which has 40 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Bupivacaine is the first listed.
NCT00508066 reports 0 study locations.
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.
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