This study will explore the efficacy and safety of a fixed dose combination of morphine and oxycodone for management of acute postoperative pain. The study will explore the efficacy dose response and dosing interval required to maintain adequate analgesia at each tested dosage strength.
This study is a randomized, double-blind, placebo-controlled, rising-dose/by-cohort study of the efficacy and safety of Q8003 in inpatients with acute pain following unilateral bunionectomy surgery. Patients in each dosing group will receive either Q8003 (approximately 50 per dosing group) or placebo (approximately 13 per dosing group), determined by random sequential assignment and blinded to patients and managing Investigators. Dosing groups will be enrolled sequentially in ascending order; only one dosing group will be open at a time for enrollment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
256
Capsules, four different mg dosage strengths
Capsules
Advanced Clinical Research Institute
Anaheim, California, United States
Chesapeake Research Group
Pasadena, Maryland, United States
Advanced Regional Center for Foot and Ankle Care
Altoona, Pennsylvania, United States
Scirex Research Center
Houston, Texas, United States
Difference in pain intensity scores from baseline
Time frame: 48 hours
Appropriate dosing interval for each tested dose level
Time frame: 48 hours
Safety: incidence of opioid-related adverse events
Time frame: 48 hours
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Lifetree Clinical Research
Salt Lake City, Utah, United States
Jean Brown Research
Salt Lake City, Utah, United States