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Study identifier: NCT05862792 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Liposomal Bupivacaine and Transoral Robotic Surgery

Condition: Oropharyngeal Cancer · Dysphagia, Oropharyngeal · Post Operative Pain  ·  Sponsor: Geisinger Clinic

PhaseN/A
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is for patients with oropharyngeal squamous cell carcinoma. We want to learn more about how we can optimize pain control in patients who undergo transoral robotic surgery (TORS) for oropharyngeal squamous cell carcinoma. Our goal is to determine if a local anesthetic called EXPAREL® (Liposomal Bupivacaine) impacts postsurgical pain and swallow function in patients with oropharyngeal squamous cell carcinoma undergoing TORS. EXPAREL® is an FDA-approved anesthetic drug that provides long-lasting and precise pain relief when injected into the surgical wound. Our study team wants to determine if injecting EXPAREL® into the surgical wound will provide better pain relief and swallow function when compared to patients who do not undergo postoperative EXPAREL® injection. Both options for postoperative pain control are considered standard of care for patients undergoing TORS.

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

Talk to the study team

Thorsen Haugen, MD  ·  570-214-7866  ·  thaugen@geisinger.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Geisinger Medical CenterDanville, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05862792