The purpose of this study to evaluate the effectiveness, safety, and tolerability of SUZ as part of multimodal therapy (MMT) in treating acute postoperative pain.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Tablets for oral administration.
Atlanta Center for Medical Research
Atlanta, Georgia, United States
Beth Israel Deaconess Medical Center - Surgery
Boston, Massachusetts, United States
HD Research LLC | First Surgical Hospital
Bellaire, Texas, United States
Memorial Hermann Village
Houston, Texas, 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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JBR Clinical Research
Salt Lake City, Utah, United States