Clinical Trial

R.E.C.K vs Exparel in Robotic Nephrectomy

Recruiting Phase 3
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Summary
The purpose of the study is to evaluate the efficacy of R.E.C.K (ropivacaine epinephrine clonidine ketorolac) vs Exparel during robotic partial and radical nephrectomy in a single institution, prospective, randomized trial. The study will evaluate post operative Numerical Rating Score (NRS) pain scores, post operative pain medication intake (opioids and over-the-counter pain medicines) and length of stay across the two patient cohorts. The findings will help to inform whether the increased cost of Exparel when compared to R.E.C.K is justified.
Protocol Amendment History 6 amendments
This ClinicalTrials.gov record has been amended 6 times since 2025-07-22; most recent amendment 2026-07-10.
Status change: Not Yet Recruiting → Recruiting 2025-11-17
Trial Details
NCT Number NCT07092566
Lead Sponsor Wake Forest University Health Sciences
Collaborators: Atrium Health Levine Cancer Institute
Conditions Renal Carcinoma, Nephrectomy / Methods, Pain Management
Enrollment 170 participants
Start Date 2025-11-14
Primary Completion 2027-10 (estimated)
Study Completion 2027-10 (estimated)
Updated on ClinicalTrials.gov 2026-07-13