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
NA
30 participants
INTERVENTIONAL
2012-01-31
2016-01-31
Brief Summary
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Detailed Description
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Study objective: To assess the value of a catheter-delivered supplementary infusion of LA to control postoperative pain after a regional block.
Hypothesis: Patients who have received a regional nerve block will experience less post-surgical pain when a second shot of LA is delivered through a perineural indwelling catheter just prior to discharge.
Study procedures: We will recruit patients who are scheduled to undergo surgery that requires a regional block of the upper extremity. We anticipate recruiting thirty individuals; the control group will receive one dose of LA using the conventional single-shot method, and the study group will be fitted with a perineural catheter through which one dose of LA will be delivered prior to surgery and another just before discharge from the hospital.
On the day of surgery, participating patients will be taken to the regional block area. Control group patients will be given a single injection of LA, under ultrasound guidance, to block the appropriate target nerve(s). These patients will undergo surgery and post-anesthesia recovery as per standard procedures. For patients in the experimental group, the attending anesthesiologist will, under ultrasound guidance, insert a perineural catheter at an appropriate location to block the target nerve. Once the catheter is in place, a single dose of LA will be delivered to block the target nerve, and the catheter will remain in the patient throughout the procedure. In the post-anesthesia recovery area, patients with a catheter will receive a second bolus infusion of the same LA. When the patient is approved for discharge, the catheter will be removed, the insertion site cleaned, and the patient will be allowed to go home.
A research assistant ask patients to rate their pain using a 0-10 numerical rating scale: 1) prior to delivery of the first dose of LA, 2) immediately following surgery (just before the second anesthetic infusion for experimental group patients), and 3) immediately before discharge from the hospital (after the second anesthetic infusion for experimental group patients). On the day after surgery, the research assistant will contact patients in both groups and will ask them to rate their pain over the 24-hour post-operative period. Pain reporting at these four time points will provide us with a comprehensive assessment of patient comfort after their regional nerve block and whether the second infusion of LA was effective at alleviating post-operative pain.
Primary outcomes:
1. Postoperative pain levels
2. Patient comfort at home
Inclusion criteria: Adult; scheduled for surgery that requires peripheral nerve blockade.
Exclusion criteria: Failure to provide informed consent; allergy to LA; neurological pathology and/or deficit in the block region.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Perineural catheter
Local anesthetic will be delivered through an indwelling perineural catheter
Perineural catheter
Patients in the experimental group will receive a single dose of local anesthetic though an indwelling catheter both before and after surgery.
Single-shot block
Local anesthetic will be delivered by the conventional, single-shot method.
Single-shot block
Patients in the control group will receive a single shot of local anesthetic, in standard fashion, before surgery.
Interventions
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Perineural catheter
Patients in the experimental group will receive a single dose of local anesthetic though an indwelling catheter both before and after surgery.
Single-shot block
Patients in the control group will receive a single shot of local anesthetic, in standard fashion, before surgery.
Eligibility Criteria
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Inclusion Criteria
* Scheduled for surgery that requires peripheral nerve blockade
Exclusion Criteria
* Allergy to local anesthetic
* Neurological pathology and/or deficit in the block region
18 Years
80 Years
ALL
No
Sponsors
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University of Alberta
OTHER
Responsible Party
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Principal Investigators
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Ban Tsui, MD, MSc
Role: PRINCIPAL_INVESTIGATOR
University of Alberta
Locations
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University of Alberta Hospital
Edmonton, Alberta, Canada
Countries
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References
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Ip VH, Tsui BC. The catheter-over-needle assembly facilitates delivery of a second local anesthetic bolus to prolong supraclavicular brachial plexus block without time-consuming catheterization steps: a randomized controlled study. Can J Anaesth. 2013 Jul;60(7):692-9. doi: 10.1007/s12630-013-9951-5. Epub 2013 May 1.
Other Identifiers
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Pro000027421
Identifier Type: -
Identifier Source: org_study_id
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