- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01615952
Patient Positioning on Supraclavicular Nerve Block
March 27, 2015 updated by: Antoun Nader, Northwestern University
Blockade of the brachial plexus using a supraclavicular approach provides excellent anesthesia for upper extremity surgery.
The most serious complication specific to this block is pneumothorax.
Subsequent modifications of this block including the use of ultrasound have lowered the risk from 6% to <1%.
Case reports remain and authors have described certain factors and strategies to reduce this risk.
Most texts and journals describe the patient in a supine or semi-sitting position during the block.
At the investigators institution the investigators perform the block in a semi-sitting position to facilitate needle tip visibility with ultrasound.
The investigators plan to obtain ultrasound anatomic measurements in three different positions (supine, semi-sitting, sitting) using patients consented for supraclavicular nerve blocks.
Study Overview
Status
Terminated
Conditions
Study Type
Observational
Enrollment (Actual)
6
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Illinois
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Chicago, Illinois, United States, 60611
- Northwestern University Feingberg School of Medicine
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients 18 y/o to 65 y/o, who are scheduled to receive a ultrasound-guided supraclavicular nerve block as part of their postoperative pain management.
Description
Inclusion Criteria:
- all patients, 18 y/o to 65 y/o, who are scheduled to receive an ultrasound- guided supraclavicular nerve block
Exclusion Criteria:
- patient refusal to be included in the study,
- the presence of language barrier that inhibits proper communication with the patient, contraindications to regional anesthesia (local infection, severe pulmonary disease, or preexisting neuropathy)
- history of allergy to amide local anesthetics or narcotics
- the presence of a progressive neurological deficit
- history of hepatorenal insufficiency
- the presence of a coagulopathy or infection
- pregnancy
- a history of psychiatric disorder
- inability to follow study protocol
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
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Sitting Position (head of bed 90 degrees)
Ultrasound measurements will be performed.
A= skin to the pleura at the level lateral to the subclavian artery, B= skin to center of the subclavian artery, C= skin to first rib, D= skin to "corner pocket"
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|
Semi-sitting position (45 degrees)
Ultrasound measurements will be performed.
A= skin to the pleura at the level lateral to the subclavian artery, B= skin to center of the subclavian artery, C= skin to first rib, D= skin to "corner pocket"
|
|
Supine position
Ultrasound measurements will be performed.
A= skin to the pleura at the level lateral to the subclavian artery, B= skin to center of the subclavian artery, C= skin to first rib, D= skin to "corner pocket"
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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patient positioning
Time Frame: Postoperative Day One
|
Ultrasound measurements will be made at three different positions: Sitting, semi-sitting, and supine.
The ultrasound measurements include A= skin to the pleura at the level lateral to the subclavian artery, B= skin to center of the subclavian artery, C= skin to first rib, D= skin to "corner pocket"
|
Postoperative Day One
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2012
Primary Completion (Actual)
November 1, 2014
Study Completion (Actual)
November 1, 2014
Study Registration Dates
First Submitted
June 7, 2012
First Submitted That Met QC Criteria
June 8, 2012
First Posted (Estimate)
June 11, 2012
Study Record Updates
Last Update Posted (Estimate)
March 30, 2015
Last Update Submitted That Met QC Criteria
March 27, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- STU00058413
- Northwestern University (Other Identifier: NU 22I05)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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