Regional anesthesia

Liposomal Bupivacaine, Plain Bupivacaine, and Saline for Transversus Abdominis Plane Blocks: The CLEVELAND Randomized Trial

AnesthesiologyPublished Randomised controlled trial

Authors' conclusion

Single-shot, four-quadrant TAP blocks performed with liposomal bupivacaine, plain bupivacaine, or normal saline before incision for various open and laparoscopic abdominal procedures resulted in similar postoperative opioid consumption and pain scores at 24, 48, and 72 h.

Study context

Population
Patients having major abdominal surgery (e.g., colorectal, gynecological, hernia repairs)modified ITT cohort
Participants
261 patients
Comparison
Liposomal bupivacaine vs Plain bupivacaine vs Placebo
  • Liposomal bupivacainen = 89
  • Plain bupivacainen = 84
  • Placebon = 88reference
Primary endpoint
Coprimary: opioid consumption (milligram morphine equivalents (MME)) during the initial 24 postoperative h, and between 24 to 48 h after surgery
Follow-up
24 h; 24 to 48 h
Methodological detailsblinded, three-arm, placebo-controlled
  • Blinded
  • Three-arm
  • Placebo-controlled

Primary result

As reported in the abstract

Opioid requirements, first 24 h · first 24 h
Each group vs placeboRatio of geometric means (97.7% CI)P value
Liposomal bupivacaine
0.86(0.60–1.24)
P = 0.355
Plain bupivacaine
0.91(0.63–1.32)
P = 0.578

Secondary outcomes

Time to sensation return, pain scores, opioid requirements 48–72 h

Similar across all groups, no significant differences

Original publication

Liposomal Bupivacaine, Plain Bupivacaine, and Saline for Transversus Abdominis Plane Blocks: The CLEVELAND Randomized Trial. Anesthesiology. Published 1 December 2025. doi:10.1097/aln.0000000000005869

Composed by AI from the published abstract and checked against it. How Briefs are made →

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