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NCT00840996 · ClinicalTrials.gov registry record · NA
Perioperative Intravenous Lidocaine or Epidural Anesthesia on Outcomes in Complex Spine Surgery
A NA study of Spine Surgery, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 116
- Enrollment target
- 1
- Study location
NCT00840996 is a NA study of Spine Surgery that has completed, run by The Cleveland Clinic. The registered enrollment target is 116 participants, below the 269-participant average among 6 other Spine Surgery trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00840996, a NA study of Spine Surgery, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 116 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is determine if epidural anesthesia administered after surgery or lidocaine administered during surgery will decrease inflammation after spinal surgery and decrease the need for post operative pain medication compared to intravenous patient controlled analgesia. Participants undergoing spine surgery will be randomized into one of two groups; \- A.) General Anesthesia and postoperative Patient Controlled Analgesia and placebo IV infusion. B.) General Anesthesia plus perioperative intravenous lidocaine infusion, and post operative Patient Controlled Analgesia.
Conditions Studied
Interventions
- DRUG placebo
- DRUG Lidocaine
Study Locations (1)
Ohio
- Cleveland Clinic - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 116 participants |
| Start Date | 2008-05 |
| Est. Completion | 2012-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00840996
The ClinicalTrials.gov registry entry for NCT00840996 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 116 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 269-participant average among 6 other Spine Surgery trials with a reported enrollment target (57% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Spine Surgery appearing as the primary indexed condition, and to 2 interventions - of which placebo is the first listed.
NCT00840996 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT00840996 about?
NCT00840996 is a clinical study titled "Perioperative Intravenous Lidocaine or Epidural Anesthesia on Outcomes in Complex Spine Surgery". The purpose of this study is determine if epidural anesthesia administered after surgery or lidocaine administered during surgery will decrease inflammation after spinal surgery and decrease the need for post operative pain medication compared to intravenous patient controlled analgesia. Participant...
What is the current status of trial NCT00840996?
This trial is currently completed. It is a NA study. The enrollment target is 116 participants. The study started on 2008-05. Estimated completion is 2012-02.
What conditions does trial NCT00840996 study?
This clinical trial studies the following conditions: Spine Surgery.
What interventions are being tested in trial NCT00840996?
The interventions under investigation include: placebo (DRUG), Lidocaine (DRUG).
Who is sponsoring clinical trial NCT00840996?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00840996 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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