Interscalene Block With and Without Liposomal Bupivacaine in Shoulder Surgery
Primary Purpose
Rotator Cuff Tear, Postoperative Pain
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Liposomal Bupivacaine
Sponsored by
About this trial
This is an interventional supportive care trial for Rotator Cuff Tear
Eligibility Criteria
Inclusion Criteria:
- Patients over 18 undergoing rotator cuff repair or total shoulder arthroplasty
Exclusion Criteria:
- Pregnant
- Documented drug of alcohol abuse
- Active narcotic use prior to surgery
- Neurological deficit
- Allergy to amide anesthetics
- Not cleared by primary care physician
- Hydrocodone or oxycodone intolerance
- Enrollment in another clinical trial or past cognitive or mental health status that interferes with study
Sites / Locations
- Greenwich Hospital
- Orthopaedic & Neurosurgery Specialists
- Stamford Ambulatory Surgical Center
- Atlantis Orthopaedics
- Atlantis Orthopaedics
- Southern Oregon Orthopedics, Inc.
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Liposomal Bupivacaine Interscalene Block
Bupivacaine Interscalene Block
Arm Description
Liposomal bupivacaine anesthetic will be administered as an interscalene block during rotator cuff repair surgery and total shoulder arthroplasty.
Bupivacaine anesthetic will be administered as an interscalene block during rotator cuff repair surgery and total shoulder arthroplasty.
Outcomes
Primary Outcome Measures
Opiate Consumption
Total amount of narcotics consumed during the postoperative period, measured in morphine equivalents (OME)
Secondary Outcome Measures
VAS Pain Scores
A standardized measure of subjective pain on a scale of 0 to 10, from zero pain to excruciating pain, respectively
Likert Pain Satisfaction Rating
A standardized measure of patient satisfaction with pain management from 1 (very unsatisfied) to 5 (very satisfied)
Full Information
NCT ID
NCT03728946
First Posted
October 31, 2018
Last Updated
March 22, 2020
Sponsor
Orthopaedic & Neurosurgery Specialists
1. Study Identification
Unique Protocol Identification Number
NCT03728946
Brief Title
Interscalene Block With and Without Liposomal Bupivacaine in Shoulder Surgery
Official Title
Interscalene Block With and Without Liposomal Bupivacaine in Shoulder Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
November 21, 2018 (Actual)
Primary Completion Date
March 1, 2020 (Actual)
Study Completion Date
March 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Orthopaedic & Neurosurgery Specialists
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to examine the difference in perioperative pain after shoulder surgery with a standard bupivacaine nerve block compared to liposomal bupivacaine enhanced nerve block alone in TSA and ARCR. Data will be compared using VAS scores and opiate consumption between the two groups. The hypothesis of this study is that an interscalene nerve block with liposomal bupivacaine will decrease both postoperative VAS pain scores and total narcotic consumption when compared to a standard bupivacaine interscalene nerve block alone.
Detailed Description
Arthroscopic rotator cuff repair (ARCR) and shoulder arthroplasty (TSA) provide excellent clinical outcomes but are often associated with significant postoperative pain, frequently managed with oral opioid medication. Orthopedic surgeons prescribe approximately 32 unused pills per shoulder surgery and are the third largest prescribers of opiates in the USA. It is incumbent upon the orthopedic community to identify postoperative pain management methods which reduce the need for narcotic medication following shoulder procedures as a means to mitigate the impact of orthopedic procedures on this epidemic.
The use of intraoperative local and regional anesthesia or field blocks, in conjunction with multimodal pharmacological strategies, is an accepted approach for managing surgical pain and reducing opiate use but requires peer reviewed protocols to gain wider acceptance.
Interscalene nerve block with bupivacaine remains a gold standard for peri-operative analgesia, but is associated with significant rebound pain due to the short duration of the local anesthetics. Recent studies have demonstrated that the addition of a liposomal bupivacaine field block may lower pain and enhance patient satisfaction throughout the first postoperative week. Liposomal bupivacaine has recently received FDA approval for ISB, but the data regarding its efficacy in nerve blocks is sparse.
The purpose of this pilot study is to determine if liposomal bupivacaine-enhanced interscalene nerve blocks can be used to improve peri-operative pain control methods, limit narcotic use, and provide appropriate postoperative analgesia compared to standard bupivacaine blocks. Primary and secondary outcome measures will be collected as number of opiates taken and self-reported VAS pain scores over a 14 day postoperative period, respectively.
The hypothesis of this study is that an interscalene nerve block with liposomal bupivacaine will decrease both postoperative VAS pain scores and total narcotic consumption when compared to a standard bupivacaine interscalene nerve block alone.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tear, Postoperative Pain
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Liposomal Bupivacaine Interscalene Block
Arm Type
Experimental
Arm Description
Liposomal bupivacaine anesthetic will be administered as an interscalene block during rotator cuff repair surgery and total shoulder arthroplasty.
Arm Title
Bupivacaine Interscalene Block
Arm Type
No Intervention
Arm Description
Bupivacaine anesthetic will be administered as an interscalene block during rotator cuff repair surgery and total shoulder arthroplasty.
Intervention Type
Drug
Intervention Name(s)
Liposomal Bupivacaine
Other Intervention Name(s)
EXPAREL
Intervention Description
Addition of 15mL of liposomal bupivacaine to 15mL of standard nerve block anesthetic solution containing 0.5% bupivacaine and 4mg of decadron
Primary Outcome Measure Information:
Title
Opiate Consumption
Description
Total amount of narcotics consumed during the postoperative period, measured in morphine equivalents (OME)
Time Frame
Post-operative days 1-14
Secondary Outcome Measure Information:
Title
VAS Pain Scores
Description
A standardized measure of subjective pain on a scale of 0 to 10, from zero pain to excruciating pain, respectively
Time Frame
Post operative days 1-14
Title
Likert Pain Satisfaction Rating
Description
A standardized measure of patient satisfaction with pain management from 1 (very unsatisfied) to 5 (very satisfied)
Time Frame
Post operative days 1-14
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients over 18 undergoing rotator cuff repair or total shoulder arthroplasty
Exclusion Criteria:
Pregnant
Documented drug of alcohol abuse
Active narcotic use prior to surgery
Neurological deficit
Allergy to amide anesthetics
Not cleared by primary care physician
Hydrocodone or oxycodone intolerance
Enrollment in another clinical trial or past cognitive or mental health status that interferes with study
Facility Information:
Facility Name
Greenwich Hospital
City
Greenwich
State/Province
Connecticut
ZIP/Postal Code
06830
Country
United States
Facility Name
Orthopaedic & Neurosurgery Specialists
City
Greenwich
State/Province
Connecticut
ZIP/Postal Code
06831
Country
United States
Facility Name
Stamford Ambulatory Surgical Center
City
Stamford
State/Province
Connecticut
ZIP/Postal Code
06902
Country
United States
Facility Name
Atlantis Orthopaedics
City
Atlantis
State/Province
Florida
ZIP/Postal Code
06831
Country
United States
Facility Name
Atlantis Orthopaedics
City
Palm Beach Gardens
State/Province
Florida
ZIP/Postal Code
33410
Country
United States
Facility Name
Southern Oregon Orthopedics, Inc.
City
Medford
State/Province
Oregon
ZIP/Postal Code
97504
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
28182507
Citation
Kumar K, Gulotta LV, Dines JS, Allen AA, Cheng J, Fields KG, YaDeau JT, Wu CL. Unused Opioid Pills After Outpatient Shoulder Surgeries Given Current Perioperative Prescribing Habits. Am J Sports Med. 2017 Mar;45(3):636-641. doi: 10.1177/0363546517693665. Epub 2017 Feb 9.
Results Reference
background
PubMed Identifier
30170012
Citation
Lee CY, Robinson DA, Johnson CA Jr, Zhang Y, Wong J, Joshi DJ, Wu TT, Knight PA. A Randomized Controlled Trial of Liposomal Bupivacaine Parasternal Intercostal Block for Sternotomy. Ann Thorac Surg. 2019 Jan;107(1):128-134. doi: 10.1016/j.athoracsur.2018.06.081. Epub 2018 Aug 28.
Results Reference
background
PubMed Identifier
28967536
Citation
Pedoto A, Amar D. Liposomal Bupivacaine for Intercostal Nerve Block: Pricey or Priceless? Semin Thorac Cardiovasc Surg. 2017 Winter;29(4):538-539. doi: 10.1053/j.semtcvs.2017.08.016. Epub 2017 Aug 30. No abstract available.
Results Reference
background
PubMed Identifier
25912739
Citation
Rice DC, Cata JP, Mena GE, Rodriguez-Restrepo A, Correa AM, Mehran RJ. Posterior Intercostal Nerve Block With Liposomal Bupivacaine: An Alternative to Thoracic Epidural Analgesia. Ann Thorac Surg. 2015 Jun;99(6):1953-60. doi: 10.1016/j.athoracsur.2015.02.074. Epub 2015 Apr 23.
Results Reference
background
PubMed Identifier
25282071
Citation
Surdam JW, Licini DJ, Baynes NT, Arce BR. The use of exparel (liposomal bupivacaine) to manage postoperative pain in unilateral total knee arthroplasty patients. J Arthroplasty. 2015 Feb;30(2):325-9. doi: 10.1016/j.arth.2014.09.004. Epub 2014 Sep 16.
Results Reference
background
PubMed Identifier
28157791
Citation
Vandepitte C, Kuroda M, Witvrouw R, Anne L, Bellemans J, Corten K, Vanelderen P, Mesotten D, Leunen I, Heylen M, Van Boxstael S, Golebiewski M, Van de Velde M, Knezevic NN, Hadzic A. Addition of Liposome Bupivacaine to Bupivacaine HCl Versus Bupivacaine HCl Alone for Interscalene Brachial Plexus Block in Patients Having Major Shoulder Surgery. Reg Anesth Pain Med. 2017 May/Jun;42(3):334-341. doi: 10.1097/AAP.0000000000000560.
Results Reference
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Interscalene Block With and Without Liposomal Bupivacaine in Shoulder Surgery
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