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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
47
Tablets for oral administration.
Scottsdale Clinical Trials
Scottsdale, Arizona, United States
Woodland International Research Group
Little Rock, Arkansas, United States
Proportion of Participants Reporting Good, Very Good, or Excellent on a Patient Global Assessment (PGA) for Pain Control at the End of Treatment
Time frame: From Day 3 up to Day 14
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