Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries (NCT06379425)
Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries: A Randomized Controlled Trial
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Northwell Health South Shore Surgery Center — Bay Shore, New York
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Northwell Health South Shore Surgery Center — Bay Shore, New York
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Pain, Postoperative
- Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery — Cincinnati, Ohio
- A Prospective Randomized Double Blind Trial to Assess the Effect of a Single Preoperative Dose of Gabapentin on Postoperative Opioid Consumption in Patients Undergoing Rhinoplasty — Columbus, Ohio
- Stopping Opioid Overuse in Obstetrics to Halt Exposure Trial — Kansas City, Missouri
- Reduced Opioid Prescription After Laparoscopic Hysterectomy — Baltimore, Maryland
- Magnesium as an Adjuvant Agent for Postoperative Pain — Cleveland, Ohio
- Personalization of Opioid Prescription Following Orthognathic Surgery — Halifax, Nova Scotia
Explore by condition: All Pain, Postoperative clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.