A Study Of Postoperative Pain Control Using An Opioid-Sparing Analgesic Pathway In Rhinologic Surgery

Overview

About this study

The purpose of this study is to prospectively evaluate postoperative pain control outcomes associated with a standardized, opioid-sparing analgesic pathway following rhinologic surgery. This study aims to determine whether effective pain management can be achieved using Suzetrigine while minimizing exposure to opioid medications. The study aligns with institutional and national opioid stewardship initiatives. All medications used in this study are part of standard clinical practice.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adults ≥18 years undergoing elective rhinologic surgery

  • Ability to provide informed consent

 

Exclusion Criteria:

  • Known contraindication to Suzetrigine

  • Chronic opioid use prior to surgery

  • Inability to complete pain assessments

  • Pregnant patients

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 05/11/2026. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Michael Marino, M.D.

Contact us for the latest status

More information

Publications

Publications are currently not available

Additional contact information

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Phone: 800-664-4542 (toll-free)

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