Use of Ultrasound in Lower Extremity Blocks.
Does Ultrasound Guidance Improve the Success of Sciatic Nerve Block at the Popliteal Fossa? A Prospective, Randomized, Controlled Trial.
1 other identifier
interventional
N/A
1 country
1
Brief Summary
Nerve "freezing" injections of the leg are very useful in providing anesthesia and pain relief for knee and ankle surgery. However, current nerve "freezing" techniques are "blind". As a result, they are not always successful and may cause complications, albeit infrequent. The objective of the current study is to determine any advantage in performing these "freezing" injections under direct ultrasound guidance, to "visualize" the nerves. We feel that by developing this technique, it will allow us to perform these procedures with greater success and fewer complications.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Feb 2003
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2005
CompletedFirst Submitted
Initial submission to the registry
September 20, 2005
CompletedFirst Posted
Study publicly available on registry
September 22, 2005
CompletedDecember 5, 2008
March 1, 2005
September 20, 2005
December 4, 2008
Conditions
Interventions
Eligibility Criteria
You may qualify if:
- English-speaking
- ASA physical status I-III
- years of age, inclusive
- kg, inclusive
- cm of height or grater
- Scheduled for elective foot or ankle surgery
You may not qualify if:
- Contraindications to sciatic nerve block (e.g., allergy to local anesthetics, coagulopathy, malignancy or infection in the popliteal area)
- Significant peripheral neuropathy or neurologic disorder affecting the lower extremity
- Pregnancy
- Contraindications to, allergies to, and/or past adverse reactions to local anesthetics
- History of alcohol or drug dependency/abuse
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Health Network, Torontolead
- University of Torontocollaborator
Study Sites (1)
University Health Network
Toronto, Ontario, M5T2S8, Canada
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anahi Perlas, MD
University Health Network, Toronto
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 20, 2005
First Posted
September 22, 2005
Study Start
February 1, 2003
Study Completion
March 1, 2005
Last Updated
December 5, 2008
Record last verified: 2005-03