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Trials / Enrolling By Invitation

Enrolling By InvitationNCT07518238

Hernia Abd Wall Recons - BDE vs Exparel

Comparative Effectiveness of Bupivacaine-Dexamethasone-Epinephrine Versus Exparel in Postoperative Outcomes for Hernia Patients Undergoing Abdominal Wall Reconstruction

Status
Enrolling By Invitation
Phase
Phase 2
Study type
Interventional
Enrollment
128 (estimated)
Sponsor
Baylor Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This trial compares how two different numbing medications help patients feel the least amount of pain while recovering from surgery.

Detailed description

This will be a prospective randomized controlled trial comparing the outcomes of hernia patients receiving BDE versus Exparel before abdominal wall reconstruction. The study will utilize the pain numeric rating scale (PNRS) validated questionnaire to assess pain levels. Patients will be asked to report their worst pain imaginable.

Conditions

Interventions

TypeNameDescription
DRUGBDE Injectable DrugBupivacaine, Dexamethasone, Epinephrine for hernia patients receiving abdominal wall reconstruction
DRUGExparel Injectable DrugExparel for hernia patients receiving abdominal wall reconstruction

Timeline

Start date
2026-01-13
Primary completion
2029-11-12
Completion
2029-11-12
First posted
2026-04-08
Last updated
2026-04-08

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07518238. Inclusion in this directory is not an endorsement.