Actively Recruiting
Transversus Abdominis Plane Blocks With Ropivacaine Continuous Infusion Catheters versus Single Dose Liposomal Bupivacaine for Pain Control After Kidney Transplant Surgery
Led by University of California, Davis · Updated on 2026-02-18
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare the pain relief effectiveness of two types of transversus abdominis plane (TAP) blocks in adults undergoing kidney transplant surgery. Specifically, it evaluates continuous ropivacaine infusion via catheters against a single dose of liposomal bupivacaine, both administered under ultrasound guidance. The study is a prospective randomized control trial conducted to better understand pain management after renal transplant operations. Participants are divided into two groups. One group receives a TAP block with a ropivacaine bolus followed by continuous infusion through a catheter placed into the TAP space, with dosing initiated at 8 ml per hour of 0.2% ropivacaine on the inpatient floor. The other group receives a single-shot TAP block using liposomal bupivacaine diluted with preservative-free saline and injected into the TAP area after initial skin infiltration with plain bupivacaine. During the study, participants' total opioid use will be measured for four days after surgery to assess pain control. Other assessments include pain scores indicating severe pain, postoperative nausea and vomiting, respiratory depression, length of hospital stay, and costs related to analgesia up to two weeks post-surgery. The trial includes close monitoring of pain and side effects, with all procedures performed under medical supervision to evaluate the analgesic effects of the interventions.
CONDITIONS
Brief Title
TAP Blocks With Ropivacaine Continuous Infusion Catheters vs Single Dose Liposomal Bupivicaine After Kidney Transplant
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients ages 18 years or older
- Renal transplant recipients
You will not qualify if you...
- Patients less than 18 years of age
- Pregnant women
- Prisoners
- Opioid tolerant patients taking more than 30 mg/day of oral morphine equivalent analgesia
- Patients on systemic anti coagulation
- Patients unable to provide consent
- Hypersensitivity to amide-type local anesthetic or any component of the drug formula
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 4 days following renal transplant surgery
Participants undergo kidney transplant surgery and receive either a TAP block with a ropivacaine continuous infusion catheter or a single dose liposomal bupivacaine TAP block for pain control.
Inpatient care during hospital stay
Duration - Up to 2 weeks following renal transplant surgery
Participants are monitored for pain control, opioid consumption, nausea, vomiting, respiratory depression, and length of hospital stay after surgery.
Approximately 6 post-operative visits during hospital stay and follow-up
Trial Site Locations
Total: 1 location
1
University of California Davis
Sacramento, California, United States, 95817
Actively Recruiting
Research Team
A
Ana Arias, BS
N
Natasha Piniero, BS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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