Hernia Abd Wall Recons - BDE vs Exparel
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- Baylor Research Institute
- Study ID
- NCT07518238
- Phase
- PHASE2
- Status
- Enrolling By Invitation
Conditions
- BDE for Hernia Patients
- Exparel for Hernia Patients
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- BDE Injectable Drug — DRUGBupivacaine, Dexamethasone, Epinephrine for hernia patients receiving abdominal wall reconstruction
- Exparel Injectable Drug — DRUGExparel for hernia patients receiving abdominal wall reconstruction
Study Details
This trial compares how two different numbing medications help patients feel the least amount of pain while recovering from surgery.
Key Dates
- Start date
- Jan 13, 2026
- Status verified
- Mar 2026
- Primary completion
- Nov 12, 2029
- Completion
- Nov 12, 2029
Study Design
- Enrollment
- 128 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: BDE for hernia patients112.5 mg of bupivacaine, 3mg dexamethasone and 0.15 mg of epinephrine. In a 30mL syringe. This will be administered into the transversus abdominis plane on both sides.
- Active Comparator: Exparel for hernia patients266mg (20ml) mixed with 30 mls of 0.25% marcaine, administered via syringe in the transversus abdominis plane on both sides.
Primary Outcome Measure
Morphine Milligram Equivalent [ Time Frame: Post-Op day 1, 2, 3, 4 and 2 Week Follow-up (Day 14) ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Baylor University Medical Center | Dallas | Texas | 75246 | - |
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