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Study identifier: NCT06233318 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Sternotomy PIFB Block in Open Heart Surgery

Condition: Autonomic Nerve Block  ·  Sponsor: Ohio State University

PhaseNA
Planned participants84
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate if the use of a bilateral nerve block with a local anesthetic (ropivacaine), as part of a standard of care pain control regimen (called multimodal analgesia \[MMA\]), has a favorable effect on our institutional MMA pain regimen. Subjects will go through the following study procedures: review of medical history and medications subjects have taken within a month prior to surgery. Subjects will be randomly assigned to one of the two study groups (1:1) to receive either, an ultrasound-guided bilateral nerve block (called "Pecto-Intercostal Fascial Block \[PIFB\]") with ropivacaine or saline 0.9 solution, in addition to our institutional MMA regimen. A baseline line pain and nausea scores will be recorded before surgery. The block will be performed right after general anesthesia induction. The details about the surgery will be collected. Pain assessments, nausea and vomiting scores will be registered at 12, 24 and 48 hours after surgery as well. Lastly, a follow up phone call will be made by the research team to conduct a pain-detect questionnaire at 30, 60 and 90 days after surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Alberto A Uribe  ·  6142930775  ·  alberto.uribe@osumc.edu

Jeremy Reeves  ·  6142933559  ·  jeremy.reeves@osumc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

The Ohio State University Wexner Medical CenterColumbus, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06233318