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NCT01407666 · ClinicalTrials.gov registry record · NA
Comparison Between Epidural and Bilateral Paravertebral Blocks in Liver Resection
A NA study, sponsored by University of Pittsburgh.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT01407666 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 100 participants.
The verdict
NCT01407666, a NA study, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
This prospective, randomized study is intended to assess the efficacy and safety of bilateral continuous paravertebral blocks compared to continuous epidural block for open liver resection. Hypotheses: Bilateral paravertebral blocks are: 1) equally effective in controlling the perioperative pain; and 2) safe, with less frequent complications following open liver resection when compared to continuous epidural block.
Interventions
- PROCEDURE paravertebral blocks
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2010-08 |
| Est. Completion | 2014-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01407666
The ClinicalTrials.gov registry entry for NCT01407666 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which paravertebral blocks is the first listed.
NCT01407666 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01407666 about?
NCT01407666 is a clinical study titled "Comparison Between Epidural and Bilateral Paravertebral Blocks in Liver Resection". This prospective, randomized study is intended to assess the efficacy and safety of bilateral continuous paravertebral blocks compared to continuous epidural block for open liver resection. Hypotheses: Bilateral paravertebral blocks are: 1) equally effective in controlling the perioperative pain; an...
What is the current status of trial NCT01407666?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2010-08. Estimated completion is 2014-11.
What interventions are being tested in trial NCT01407666?
The interventions under investigation include: paravertebral blocks (PROCEDURE).
Who is sponsoring clinical trial NCT01407666?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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