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A Phase 4, Open-label, Single-arm Study Evaluating the Effectiveness and Safety of Suzetrigine As Part of Multimodal Therapy for Acute Pain After Laparoscopic Procedures of the Intraperitoneal or Retroperitoneal Cavities or Arthroscopic Orthopedic Procedures
The purpose of this study is to evaluate the effectiveness, safety, and tolerability of SUZ for acute pain after laparoscopic procedures of the intraperitoneal or retroperitoneal cavities or arthroscopic orthopedic procedures.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Scottsdale Clinical Trials
Scottsdale, Arizona, United States
Woodland International Research Group
Little Rock, Arkansas, United States
Gulfcoast Research Institute
Sarasota, Florida, United States
MedStar
Baltimore, Maryland, United States
Oasis Clinical Research
Las Vegas, Nevada, United States
Cooper University HealthCare (CUH)
Camden, New Jersey, United States
North Shore University Hospital - Anesthesiology
Manhasset, New York, United States
OrthoCarolina - Hip & Knee Center
Charlotte, North Carolina, United States
Eximia Research-Durham
Durham, North Carolina, United States
Duke University Hospital - Anesthesiology
Durham, North Carolina, United States
Start Date
March 27, 2025
Primary Completion Date
October 27, 2025
Completion Date
November 10, 2025
Last Updated
December 15, 2025
47
ACTUAL participants
Suzetrigine
DRUG
Lead Sponsor
Vertex Pharmaceuticals Incorporated
NCT07422272
NCT07310953
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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