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"The Efficacy of Exparel Versus a Multidrug Cocktail in Soft Tissue Tumors"

Primary Purpose

Musculoskeletal Diseases, Soft Tissue Mass

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Exparel Injectable Product
Multi-Drug Cocktail (Ropivicaine, Epinephrine, Ketolorac, Clonidine)
Sponsored by
Morristown Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Musculoskeletal Diseases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All primary soft tissue tumors
  • Any adult patient (over 18 years old) with a soft tissue tumor confirmed with advanced imaging.

Two different study groups will be examined:

  • Those patients undergoing resection of their soft tissue tumor intraoperatively injected with Exparel
  • Those patients undergoing resection of their soft tissue tumor intraoperatively injected with the cocktail.
  • Those two groups will be further stratified by anatomic location; Upper vs lower extremity, size; tumors ≥ 10cm, tumors ≥ 5cm, tumors < 5cm, and depth; superficial vs deep.

Exclusion Criteria:

  • Pediatric Patients
  • Patients without soft tissue tumors
  • Tylenol or oxycodone allergy

Sites / Locations

  • Morristown Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Exparel Group

Multi-Drug Cocktail Group

Arm Description

70 subjects will receive Exparel

70 subjects will receive a Multi-drug Cocktail

Outcomes

Primary Outcome Measures

Pain Outcomes
Pain will be recorded on a sheet for each patient. Self-reported, patient will describe pain each day on a scale of 1-10 (10 being the worst)

Secondary Outcome Measures

Medication Consumption
Patient will self-report how much medication he or she took each day post-operatively.

Full Information

First Posted
April 7, 2022
Last Updated
April 27, 2022
Sponsor
Morristown Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05355597
Brief Title
"The Efficacy of Exparel Versus a Multidrug Cocktail in Soft Tissue Tumors"
Official Title
"The Efficacy of Exparel Versus a Multidrug Cocktail in Soft Tissue Tumors"
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 27, 2021 (Actual)
Primary Completion Date
July 7, 2023 (Anticipated)
Study Completion Date
July 7, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Morristown Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this proposed project is to determine which local anesthetic is more efficacious for use in soft tissue tumors: Exparel (liposomal bupivacaine) or a cocktail of Ropivicaine, Epinepherine, Ketolorac and Clonidine. This study will examine patients' post-operative pain levels as well as their narcotic consumption after removal of a soft tissue tumor while hospitalized and then twice daily through postoperative day 14.
Detailed Description
In recent years, there has been a substantial push to create a post-surgical protocol consisting of multimodal analgesia across multiple surgical subspecialties to decrease narcotic consumption and cost1. The negative side effects of narcotics and their addiction potential are well understood. One of the modes of analgesia currently in use to mitigate surgical pain is some form of local anesthetic. Increasing the duration of analgesia has been sought after since its inception. Subsequently, longer acting anesthetics like bupivacaine have been implemented as well as supplementing their use with other drugs, such as epinephrine, to increase their effect duration and overall efficacy2. This has led to the development of Liposomal Bupivicaine or Exparel (TM, Parsippany NJ etc.) Exparel works by infusing liposomes in the administration of the long acting local analgesic which entrap the biologically active drug and slowly release it over a period of 72-96 hours 3-4. Thus, post-operative pain can be managed via direct injection of the drug at the surgical site with upwards to four days of pain relief. Exparel has been studied extensively in the surgical literature; although within orthopedics, it has been primarily in regard to arthroplasty5. There has yet to be a study to illicit the best form of post-operative pain control in the world of orthopedic oncology, specifically in soft tissue tumors. The objective of this proposed project is to determine which local anesthetic is more efficacious for use in soft tissue tumors: Exparel (liposomal bupivacaine) or a cocktail of Ropivicaine, Epinepherine, Ketolorac and Clonidine. This study will examine patients' post-operative pain levels as well as their narcotic consumption after removal of a soft tissue tumor while hospitalized and then twice daily through postoperative day 14.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Musculoskeletal Diseases, Soft Tissue Mass

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Total of 140 subjects are recruited. Group A Receives one drug (70) and Group B receives the other drug (70)
Masking
ParticipantCare Provider
Masking Description
This a double blinded study in which the investigator nor subjects will know which drug he or she receives.
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exparel Group
Arm Type
Experimental
Arm Description
70 subjects will receive Exparel
Arm Title
Multi-Drug Cocktail Group
Arm Type
Experimental
Arm Description
70 subjects will receive a Multi-drug Cocktail
Intervention Type
Drug
Intervention Name(s)
Exparel Injectable Product
Intervention Description
Both drugs have same desired effect. Will be injected intra-operatively while subjects are under anesthesia to alleviate significant post-operative pain.
Intervention Type
Drug
Intervention Name(s)
Multi-Drug Cocktail (Ropivicaine, Epinephrine, Ketolorac, Clonidine)
Intervention Description
Same desired effect as Exparel but different mechanism of action. Will be injected intra-operatively while subjects are under anesthesia to alleviate significant post-operative pain.
Primary Outcome Measure Information:
Title
Pain Outcomes
Description
Pain will be recorded on a sheet for each patient. Self-reported, patient will describe pain each day on a scale of 1-10 (10 being the worst)
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Medication Consumption
Description
Patient will self-report how much medication he or she took each day post-operatively.
Time Frame
14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All primary soft tissue tumors Any adult patient (over 18 years old) with a soft tissue tumor confirmed with advanced imaging. Two different study groups will be examined: Those patients undergoing resection of their soft tissue tumor intraoperatively injected with Exparel Those patients undergoing resection of their soft tissue tumor intraoperatively injected with the cocktail. Those two groups will be further stratified by anatomic location; Upper vs lower extremity, size; tumors ≥ 10cm, tumors ≥ 5cm, tumors < 5cm, and depth; superficial vs deep. Exclusion Criteria: Pediatric Patients Patients without soft tissue tumors Tylenol or oxycodone allergy
Facility Information:
Facility Name
Morristown Medical Center
City
Morristown
State/Province
New Jersey
ZIP/Postal Code
07960
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
tyler hoskins, BA
Phone
201-394-6735
Email
tyler.hoskins@atlantichealth.org

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual Participant Data will not be shared with other researchers, but we do anticipate publishing the results in a journal.
Citations:
PubMed Identifier
26447431
Citation
Kelly MA. Current Postoperative Pain Management Protocols Contribute to the Opioid Epidemic in the United States. Am J Orthop (Belle Mead NJ). 2015 Oct;44(10 Suppl):S5-8.
Results Reference
result
PubMed Identifier
22285545
Citation
Bramlett K, Onel E, Viscusi ER, Jones K. A randomized, double-blind, dose-ranging study comparing wound infiltration of DepoFoam bupivacaine, an extended-release liposomal bupivacaine, to bupivacaine HCl for postsurgical analgesia in total knee arthroplasty. Knee. 2012 Oct;19(5):530-6. doi: 10.1016/j.knee.2011.12.004. Epub 2012 Jan 28.
Results Reference
result
PubMed Identifier
2674208
Citation
Ranade VV. Drug delivery systems. 1. site-specific drug delivery using liposomes as carriers. J Clin Pharmacol. 1989 Aug;29(8):685-94. doi: 10.1002/j.1552-4604.1989.tb03403.x.
Results Reference
result
PubMed Identifier
26447426
Citation
Barrington JW. Efficacy of Periarticular Injection With a Long-Acting Local Analgesic in Joint Arthroplasty. Am J Orthop (Belle Mead NJ). 2015 Oct;44(10 Suppl):S13-6.
Results Reference
result

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"The Efficacy of Exparel Versus a Multidrug Cocktail in Soft Tissue Tumors"

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