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NCT00876746 · ClinicalTrials.gov registry record · Phase 4
Optimization of Catheter Insertion Site for Continuous Peripheral Nerve Blocks
A Phase 4 study of Post Operative Pain and Upper-extremity Surgery, sponsored by University of California, San Diego.
- Completed
- Registry status
- Phase 4
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT00876746 is a Phase 4 study of Post Operative Pain and Upper-extremity Surgery that has completed, run by University of California, San Diego. The registered enrollment target is 60 participants, below the 235-participant average among 56 other Post Operative Pain trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00876746, a Phase 4 study of Post Operative Pain and Upper-extremity Surgery, has completed, sponsored by University of California, San Diego.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
This research study is to determine if the insertion site of a perineural catheter or tiny tube placed next to the nerves that go to the part of the body (hand or arm) having surgery, affects the amount of pain relief that is experienced after surgery. Catheters will be placed in either the supraclavicular or infraclavicular location.
Conditions Studied
Interventions
- PROCEDURE Supraclavicular vs. Infraclavicular ropivicaine infusion
Study Locations (1)
California
- UCSD Medical Center - San Diego
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2008-12 |
| Est. Completion | 2010-01 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00876746
The ClinicalTrials.gov registry entry for NCT00876746 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, below the 235-participant average among 56 other Post Operative Pain trials with a reported enrollment target (74% lower). The listed sponsor is University of California, San Diego, which has 775 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 1 intervention - of which Supraclavicular vs. Infraclavicular ropivicaine infusion is the first listed.
NCT00876746 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT00876746 about?
NCT00876746 is a clinical study titled "Optimization of Catheter Insertion Site for Continuous Peripheral Nerve Blocks". This research study is to determine if the insertion site of a perineural catheter or tiny tube placed next to the nerves that go to the part of the body (hand or arm) having surgery, affects the amount of pain relief that is experienced after surgery. Catheters will be placed in either the supracla...
What is the current status of trial NCT00876746?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2008-12. Estimated completion is 2010-01.
What conditions does trial NCT00876746 study?
This clinical trial studies the following conditions: Post Operative Pain, Upper-extremity Surgery.
What interventions are being tested in trial NCT00876746?
The interventions under investigation include: Supraclavicular vs. Infraclavicular ropivicaine infusion (PROCEDURE).
Who is sponsoring clinical trial NCT00876746?
This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00876746 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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