Skip to content

Pain Control in Bariatric Patients: EXPAREL(R) vs. the On-Q(R) Pain Ball

Pain Control in Bariatric Patients: A Prospective Trial Comparing the Effectiveness of EXPAREL(R) Versus the On-Q(R) Pain Ball

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02142829
Enrollment
101
Registered
2014-05-20
Start date
2012-11-30
Completion date
2013-03-31
Last updated
2014-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

bariatric surgery, postoperative pain

Brief summary

This study was conducted to compare the effectiveness of two local pain control methods in bariatric patients by assessing the amount of postoperative pain and amount of postoperative pain medications needed. This information was used to determine which local anesthetic provided the best pain control.

Detailed description

The investigators have previously utilized the On-Q® pain ball to obtain local control by continuous delivery of bupivacaine to pain fibers at the incision site. On-Q makes use of an implanted catheter and a continuous infusion pump that the patient carries with them typically for 48-72 hours after surgery. EXPAREL is a long-acting liposomal delivery vehicle that extends the life of bupivacaine in the surgical site for up to 72 hours. It can be injected in all trocar sites and offers another potential solution to patient pain control without the need for a catheter and the hardware needed to deliver the local anesthetic. Patient NRS (numerical rating scale) scores for postoperative pain and total medication consumed were used to assess the differences between the two treatment groups.

Interventions

DRUGEXPAREL
DRUGOn-Q Pain Ball

bupivacaine HCl 0.25%

Sponsors

Pacira Pharmaceuticals, Inc
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-80, male or female

Exclusion criteria

* Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Numeric rating scale (NRS) pain intensity scores4-6 hours postoperatively and in the mornings of postoperative Day 1 and Day 2The NRS was from 0 = no pain and 10 = worst pain.

Secondary

MeasureTime frame
Postoperative opioid consumption1 week

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026