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NCT07821931
Suzetrigine in Tonsillectomy for Opioid-sparing Pain Management
Conditions: Tonsillectomy, Pharyngoplasty, Suzetrigine, Opioid, Postoperative Pain, Acute Pain
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 58
Sponsor: Stanford University
Location: Stanford University Palo Alto California
Summary
The goal of this clinical trial is to learn if a non-opioid pain medicine called suzetrigine can lower how much opioid pain medicine adults need after tonsil surgery (tonsillectomy) or a similar throat surgery.
Eligibility Criteria
Inclusion Criteria:
1. Scheduled to undergo tonsillectomy or a variant pharyngeal procedure (e.g., palatoplasty, uvulopalatopharyngoplasty \[UPPP\], expansion sphincter pharyngoplasty \[ESP\]) by a study investigator.
2. Able to understand the consent discussion in English by telephone, provide informed consent, and comply with study procedures, including completion of electronic patient-reported outcome surveys.
3. Willing and able to complete daily electronic (text message and/or email) pain surveys for 14 days and to return the dispensed opioid bottle for pill count or to respond to a telephone pill-count contact.
Exclusion Criteria:
1. Chronic opioid use
2. Significant hepatic disease
3. Pregnant or breastfeeding.
4. Known allergy or intolerance to any study medication
5. Unable to complete patient-reported outcome measures because of language barrier, literacy, or infirmity.
6. Current use of a strong CYP3A4 inhibitor
7. Use of hormonal birth control and unwilling to receive suzetrigine-related counseling, given that suzetrigine may reduce hormonal contraceptive efficacy.
Source: ClinicalTrials.gov (NCT07821931). StuddyBuddy aggregates publicly available trial information.