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 — DRUG
    Bupivacaine, Dexamethasone, Epinephrine for hernia patients receiving abdominal wall reconstruction
  • Exparel Injectable Drug — DRUG
    Exparel 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 patients
    112.5 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 patients
    266mg (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)

FacilityCityStateZIPSite coordinators
Baylor University Medical CenterDallasTexas75246-

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