A Study Comparing Continuous Sciatic Nerve Block to Single Shot Sciatic Nerve Block
Stopped early · Phase 4
Conditions studied: Fracture of Foot
In brief
The purpose of this study is to compare the incidence of postoperative symptoms of neurologic injury after a single shot infragluteal-parabiceps sciatic nerve block versus a continuous infragluteal-parabiceps sciatic nerve catheter.
Key facts
- Study ID
- NCT01615939
- Run by
- Northwestern University
- People needed
- 17
- Starts
- 2012-06-01
- Expected to finish
- 2015-01-01
- Last updated by the study team
- 2016-08-01
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- all patients ( ≥18 and ≤ 80) who are scheduled to undergo elective scheduled foot surgery and agreed to receive a sciatic nerve catheter as a part of their postoperative pain management. this study.
You may not qualify if…
- history of hemostatic abnormalities
- chronic pain syndrome
- a foot deformity restricting normal foot movement
- severe liver or renal disease
- a preexisting neurologic disorder
- patient refusal to participate
- the presence of language barrier that prohibits proper communication with patient.
Where it is running
- Northwestern University Feinberg School of Medicine — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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