This is a double-arm randomized control trial evaluating the impact of preoperative opioid-free analgesia on time to trial of void in ambulatory urogynecologic surgeries. The investigators hypothesize that receipt of acetaminophen, celecoxib and gabapentin preoperatively versus acetaminophen alone will reduce the time to trial of void in patients undergoing same-day minor urogynecologic procedures.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
70
Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery
Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery
Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery
Northwell Health South Shore Surgery Center
Bay Shore, New York, United States
RECRUITINGTime to initiation of active trial of void
Time frame: through study completion, an average of 2 years
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