Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries
Sponsor: Northwell Health • ClinicalTrials.gov ID: NCT06379425
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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.
Interventions
-
Acetaminophen
(Drug)
Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery
-
Celecoxib
(Drug)
Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery
-
Gabapentin
(Drug)
Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery
Eligibility criteria
Conditions
Locations
- Northwell Health South Shore Surgery Center — Bay Shore, New York, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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