RecruitingPhase 4NCT06379425

Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries

Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries: A Randomized Controlled Trial

Sponsor

Northwell Health

Enrollment

70 participants

Start Date

Mar 1, 2024

Study Type

INTERVENTIONAL

Conditions

Pain, Postoperative Postoperative Pain, Acute

Summary

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.

Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Acetaminophen, a drug called Celecoxib, and others for people with pain, postoperative and postoperative pain, acute. The study is currently recruiting participants at 1 location. People eligible for this study include women.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAcetaminophen

Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery

DRUGCelecoxib

Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery

DRUGGabapentin

Will add additional medications celecoxib and gabapentin to acetaminophen preoperatively prior to patient surgery

Locations(1)

Northwell Health South Shore Surgery Center

Bay Shore, New York, United States

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NCT06379425

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