Sprix for Postoperative Pain Control Following Gynecologic Surgery

Surgery Clinical Trial

Official title: Can Intranasal Ketorolac Tromethamine Prescribed Postoperatively After Major Female Pelvic Reconstructive Surgery Reduce Consumption of Prescribed Narcotics?

Status Withdrawn

Clinical Trial Summary

The ongoing opioid epidemic has altered both how physicians prescribe narcotics and patients' perceptions of those prescriptions. Along with increased scrutiny regarding the quantity of opioids that be may prescribed after acute injury, for chronic conditions and following surgery the healthcare industry as a whole continues to search for alternative medications that provide adequate pain relief and have a reduced tendency for abuse/dependence/addition. To that end this study has the following aims:

1. To evaluate the amount of opioids consumed following minimally invasive, female pelvic surgery when patients' postoperative pain is managed via:

1. Acetaminophen plus Ibuprofen plus breakthrough pain opioids (Standard protocol)

2. Acetaminophen plus Intranasal Ketorolac Tromethamine plus opioids for breakthrough pain (Sprix protocol)

2. Patient satisfaction with the aforementioned methods

3. Evaluate and compare pain scores via validated questionnaire

Hypothesis:

Primary:

1. Patients prescribed intranasal Ketorolac (Sprix protocol) will consume significantly less Morphine Milliequivalents (mEqs) of narcotics compared to the standard protocol following minimally invasive female pelvic surgery.

Secondary:

1. Patients in the Sprix protocol will have lower Visual Analog Scale (VAS) measures of pain which will be measured on a 0-10 scale where 0 denotes no pain and 10 denotes maximum experience of pain

2. Patients in the Sprix protocol will have lower numeric pain score and on POD#4

3. Patients in the Sprix protocol will have higher Quality of Recovery 40 (QoR-40 )scores on POD#1

4. Patients in the Sprix protocol will have higher QoR-40 scores on POD#4

5. Patients will not have any significant difference in overall surgical satisfaction on POD#1 and POD#4 using a numerical satisfaction score

6. Patients in the Sprix protocol will be more likely to consume no narcotics at all once discharged to home

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Enuresis
• Narcotic Use
• Pain, Postoperative
• Pelvic Organ Prolapse
• Post Operative Pain Control
• Prolapse
• Surgery
• Urinary Incontinence
• Urinary Incontinence , Stress
• Urinary Incontinence, Stress

• NCT number: NCT04444830
• Study type: Interventional
• Source: University of Louisville
• Status: Withdrawn
• Phase: Phase 4
• Start date: January 2021
• Completion date: September 21, 2021