This is a randomized, double-blind, multicenter, fixed dose factorial study of Q8003 12 mg/8 mg and Q8003 6 mg/4 mg versus its individual morphine sulfate and oxycodone hydrochloride components for the management of acute moderate to severe postoperative pain following bunionectomy surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
197
One Q8003 (morphine sulfate and oxycodone HCl) 12mg/8mg IR Capsule q6h
One morphine sulfate 12mg IR capsule q6h
One oxycodone HCl 8mg IR Capsule q6h
Associated Foot and Ankle Specialists
Phoenix, Arizona, United States
Advanced Clinical Research Institute
Anaheim, California, United States
Crossroads Research, Inc.
Owings Mills, Maryland, United States
Chesapeake Foot and Ankle
Pasadena, Maryland, United States
Difference in pain intensity scores from baseline
Time frame: 48 hours
Safety: adverse events
Time frame: 48 hours
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One Q8003 (morphine sulfate and oxycodone HCl) 6mg/4mg IR Capsule q6h
Two morphine sulfate 3mg IR capsules q6h
Two oxycodone HCl 2mg IR Capsules q6h
Advanced Regional Center for Ankle and Foot Care
Altoona, Pennsylvania, United States
Jean Brown Research
Salt Lake City, Utah, United States