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A Randomized Trial of Exparel vs Saline in Opioid Reduction of Pain Management Following Lumbar Spine Surgeries.

University of Missouri (MU) logo

University of Missouri (MU)

Status and phase

Completed
Phase 4

Conditions

Lumbar Spine Degeneration

Treatments

Drug: saline 0.9%
Drug: Liposomal bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT04644796
2037544

Details and patient eligibility

About

The purpose of this study is to establish a relationship between liposomal bupivacaine surgical site injection and postop opioid utilization.

Full description

Multiple studies have shown that people who are taking opioids for acute pain have a greater likelihood of long-term opioid use. Many efforts have been made to reduce postop pain and opioid use, including developments in incisional site injections of local anesthetics, continuous incisional site anesthetic pain pumps, as well as multimodal comprehensive pain management, yet patients undergoing lumbar spine surgeries continue to depend on opioids for relief. Liposomal bupivacaine (LB) (Exparel) is a novel formulation of long-acting bupivacaine, lasting for up to 72 hours following injection. LB has been shown to be efficacious in reducing postop pain and opioid utilization in several different surgical settings, however its utility in spine surgeries has still yet to be established. The goal of this study is to determine the efficacy of liposomal bupivacaine vs saline in lumbar spine surgeries in reducing opioid utilization as well as determine if there difference patient reported outcomes and length of hospital stay.

Enrollment

34 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing isolated lumbar spine procedures using a posterior approach.
  • Surgical spine procedures include:
  • Single-level lumbar spine surgeries with or without fusion
  • Multi-level lumbar spine surgeries with or without fusion

Exclusion criteria

  • Procedures involving intrathecal space
  • Patients with documented allergy to local anesthetics (bupivacaine, lidocaine, procaine, benzocaine).
  • Acute lumbar trauma that requires immediate spine stabilization
  • Revision of failed back surgeries (including nonunion and malunion)
  • Revision of wound or hardware
  • Contraindication to regional anesthesia
  • Patients with chronic use of opioid medications
  • Liver dysfunction (INR > 1.5, albumin <2.8g/dl, bilirubin >2mg/dl)
  • Renal dysfunction (eGFR < 60ml/min/1.73m2)
  • Severe chronic obstructive pulmonary disease requiring continuous oxygen supplementation
  • Unable to give informed consent
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

34 participants in 2 patient groups, including a placebo group

Placebo Group
Placebo Comparator group
Description:
Patients in this group will be given the placebo (sterile saline).
Treatment:
Drug: saline 0.9%
Liposomal bupivacaine
Active Comparator group
Description:
Patients in this group will be given the study drug (liposomal bupivacaine).
Treatment:
Drug: Liposomal bupivacaine

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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