Ultrasound-Guided Continuous Sciatic Nerve Blocks: Popliteal Versus Subgluteal Catheters
NCT ID: NCT01325012
Last Updated: 2013-03-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
PHASE4
2 participants
INTERVENTIONAL
2011-03-31
2013-03-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Subgluteal Sciatic Nerve Block
Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the subgluteal location 1-3 cm caudad to the inferior border of the gluteus maximus muscle.
Subgluteal Sciatic Nerve Block
Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the subgluteal location 1-3 cm caudad to the inferior border of the gluteus maximus muscle. After catheter placement, outcome measures will be assessed.
Popliteal Sciatic Nerve Block
Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the popliteal location 1-3 cm cephalad to the sciatic bifurcation.
Popliteal Sciatic Nerve Block
Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the popliteal location 1-3 cm cephalad to the sciatic bifurcation. After Catheter placement outcome measures will be assessed.
Interventions
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Subgluteal Sciatic Nerve Block
Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the subgluteal location 1-3 cm caudad to the inferior border of the gluteus maximus muscle. After catheter placement, outcome measures will be assessed.
Popliteal Sciatic Nerve Block
Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the popliteal location 1-3 cm cephalad to the sciatic bifurcation. After Catheter placement outcome measures will be assessed.
Eligibility Criteria
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Inclusion Criteria
* spending the first postoperative night hospitalized
* age 18 years or older
Exclusion Criteria
* inability to communicate with the investigators and hospital staff
* incarceration
* clinical neuropathy in the surgical extremity
18 Years
ALL
No
Sponsors
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University of California, San Diego
OTHER
Responsible Party
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Brian M. Ilfeld, MD, MS
Associate Professor, In Residence
Principal Investigators
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Brian M Ilfeld, M.D., M.S.
Role: PRINCIPAL_INVESTIGATOR
University of California, Department of Anesthesiology
Locations
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UCSD Medical Center, Thornton
La Jolla, California, United States
UCSD Medical Center Hillcrest
San Diego, California, United States
Countries
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Other Identifiers
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Subgluteal vs Popliteal
Identifier Type: -
Identifier Source: org_study_id