A Pain Relief Trial Utilizing the Infiltration of a Multivesicular Liposome Formulation Of Bupivacaine, EXPAREL®: A Phase 4 Health Economic Trial in Adult Patients Undergoing Open Colectomy
Overview
- Phase
- Phase 4
- Intervention
- IV morphine sulfate
- Conditions
- Bowel Obstruction
- Sponsor
- Pacira Pharmaceuticals, Inc
- Enrollment
- 5
- Locations
- 1
- Primary Endpoint
- Health Economic Benefits
- Status
- Terminated
- Last Updated
- 12 years ago
Overview
Brief Summary
This study is designed to compare the standard of care against EXPAREL (bupivacaine liposome extended-release injectable suspension) to determine if total opioid consumption is reduced when using EXPAREL, therefore possibly reducing total hospitalization costs.
Detailed Description
This is a phase 4, prospective, sequential, open-label study designed to evaluate the efficacy, safety, and health economic benefits of intraoperative local wound infiltration with EXPAREL (bupivacaine liposome extended-release injectable suspension), compared with postsurgical administration of standardized intravenous (IV) morphine sulfate, for postsurgical analgesia in adult patients undergoing open colectomy with general anesthesia.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or female, 18 years of age or older.
- •Patients scheduled to undergo open segmental colectomy with planned primary anastamosis, as defined by cecectomy, right hemicolectomy, resection of transverse colon, left hemicolectomy, or sigmoidectomy.
- •Ability to provide informed consent, adhere to study visit schedule, and complete all assessments.
Exclusion Criteria
- •Patients with a history of hypersensitivity or idiosyncratic reactions or intolerance to any local anesthetic, opioid, or propofol.
- •Patients who abuse alcohol or other drug substance.
- •Patients with severe hepatic impairment.
- •Patients currently pregnant or who may become pregnant during the course of the study.
- •Patients with any psychiatric, psychological, or other condition that the Investigator feels may make the patient an inappropriate candidate for this clinical study.
- •Patients who have participated in a EXPAREL study within the last 30 days.
- •Patients who have received an investigational drug within 30 days prior to study drug administration, or planned administration of another investigational product or procedure during the patient's participation in this study.
- •Patients who undergo any concurrent surgical procedure during the ileostomy reversal surgery.
- •In addition, the patient will be ineligible if he/she meets the following criteria during surgery:
- •Patients with unplanned multiple segmental resections or large intestine.
Arms & Interventions
IV morphine sulfate
morphine sulfate (or Sponsor-approved equivalent)
Intervention: IV morphine sulfate
EXPAREL
EXPAREL (bupivacaine liposome injectable suspension)
Intervention: EXPAREL (bupivacaine liposome injectable suspension)
Outcomes
Primary Outcomes
Health Economic Benefits
Time Frame: Wound closure to Day 30
1. Total cost of hospitalization until the time hospital discharge order is written or through Day 30, whichever is sooner. 2. Length of stay (LOS), recorded in hours, defined as the time of completion of the wound closure until the hospital discharge order is written or through Day 30, whichever is sooner.
Total Opioid Burden
Time Frame: Wound closure to time hospital discharge order written or Day 30, whichever is sooner
Total opioid consumed (IV and PO) postsurgically until the hospital discharge order is written or through Day 30, whichever is sooner.
Secondary Outcomes
- Incidence of Opioid-related Adverse Events and Patient Satisfaction With Postsurgical Analgesia.(Wound closure to time hospital discharge order written or Day 30, whichever is sooner.)