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NCT01916590 · ClinicalTrials.gov registry record · NA
Effectiveness of Continuous Femoral Nerve Block Versus Single Shot Femoral Nerve Block for Pain Control
A NA study, sponsored by University of Colorado, Denver.
- Terminated
- Registry status
- NA
- Development phase
- 7
- Enrollment target
NCT01916590 is a NA study that was terminated before completion, run by University of Colorado, Denver. The registered enrollment target is 7 participants.
The verdict
NCT01916590, a NA study, was terminated before completion, sponsored by University of Colorado, Denver.
- TERMINATED
- Registry status
- NA
- Development phase
- 7 participants
- Enrollment target
Study Summary
Both single shot femoral nerve block and continuous femoral nerve block with catheter have been shown to be effective for pain control after anterior cruciate ligament reconstruction (ACLR). Continuous femoral nerve block may be the more effective of the two in reducing pain scores and opioid consumption for the first 48 hours postoperatively.
Interventions
- DRUG placebo
- DRUG Bupivicaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2011-07 |
| Est. Completion | 2014-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01916590
The ClinicalTrials.gov registry entry for NCT01916590 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT01916590 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01916590 about?
NCT01916590 is a clinical study titled "Effectiveness of Continuous Femoral Nerve Block Versus Single Shot Femoral Nerve Block for Pain Control". Both single shot femoral nerve block and continuous femoral nerve block with catheter have been shown to be effective for pain control after anterior cruciate ligament reconstruction (ACLR). Continuous femoral nerve block may be the more effective of the two in reducing pain scores and opioid consum...
What is the current status of trial NCT01916590?
This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2011-07. Estimated completion is 2014-05.
What interventions are being tested in trial NCT01916590?
The interventions under investigation include: placebo (DRUG), Bupivicaine (DRUG).
Who is sponsoring clinical trial NCT01916590?
This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.
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