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Clinical Trials/NCT05355597
NCT05355597
Terminated
Phase 2

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

Atlantic Health System1 site in 1 country116 target enrollmentJanuary 27, 2021

Overview

Phase
Phase 2
Intervention
Exparel Injectable Product
Conditions
Musculoskeletal Diseases
Sponsor
Atlantic Health System
Enrollment
116
Locations
1
Primary Endpoint
Pain Outcomes
Status
Terminated
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 27, 2021
End Date
March 24, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

James Wittig

Dr.

Atlantic Health System

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

Arms & Interventions

Exparel Group

70 subjects will receive Exparel

Intervention: Exparel Injectable Product

Multi-Drug Cocktail Group

70 subjects will receive a Multi-drug Cocktail

Intervention: Multi-Drug Cocktail (Ropivicaine, Epinephrine, Ketolorac, Clonidine)

Outcomes

Primary Outcomes

Pain Outcomes

Time Frame: 14 days

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 Outcomes

  • Medication Consumption(14 days)

Study Sites (1)

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