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
| Type | Name | Description |
|---|---|---|
| DRUG | BDE Injectable Drug | Bupivacaine, Dexamethasone, Epinephrine for hernia patients receiving abdominal wall reconstruction |
| DRUG | Exparel Injectable Drug | Exparel 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07518238. Inclusion in this directory is not an endorsement.