Efficacy of IV Acetaminophen in Acute Post-Operative Pain Control in Laparoscopic Roux-en-Y Gastric Bypass Surgery (LRYGBP) Patients

Not Applicable

• Conditions: Morbid Obesity
• Interventions: Drug: IV acetaminophen; Drug: IV normal saline

• Registration Number: NCT01460667
• Lead Sponsor: McLaren Regional Medical Center

Brief Summary

Laparoscopic Roux-en-Y gastric bypass (LRYGBP) is a common type of surgery in which length of stay and morbidity is intimately associated with post-operative nausea and vomiting (PONV) and recovery of bowel function. Medications most commonly used to control for post-operative pain are opioid medications, whose well known adverse effects include PONV. Currently, no studied adequate alternative to opiates exists for mild-moderate pain relief without the aforementioned risks.

The primary goal for this study is to evaluate the the administration of pre- and post-operative IV acetaminophen to determine if there is in an overall decrease in the use of opioid analgesics by patient controlled analgesia (PCA) and subsequent decrease in subjective PONV leading to sooner return of bowel function, enabling progression to oral intake and decrease in post-operative length of stay.

Detailed Description

Opioid use during the post-operative period is a highly effective means of treatment for acute pain, however not without its adverse effects including post-operative nausea, vomiting (PONV), constipation, urinary retention, sedation and respiratory depression. Such factors have been implied in the literature to contribute to prolonged post-operative length of stay, delayed return to diet, return of bowel function and increased incidence of ileus. Alternatively, non-opioids, such as acetaminophen, aspirin, NSAIDs, and selective cyclo-oxygenase-2 inhibitors, can be utilized for acute pain, either alone or in combination with opioids. In the bariatric post-surgical population, NSAIDS both oral and IV (Toradol, Ibuprofen) are not recommended due to their potential bleeding tendency, anti-inflammatory effect, and ulcerogenic effect.

The LRYGBP may be classified as a surgery type associated with mild to moderate post-operative pain. Therefore, the mode of pain relief could directly affect the length of stay. The advent of IV acetaminophen serves as a opportunity to investigate in detail the efficacy of this non-opioid medication in the management of acute pain in the immediate post-operative period without the aforementioned adverse effects as expected from traditional opiate medications. A comprehensive approach to this study includes a prospective, double-blinded, randomized controlled trial of subjects who will undergo LRYGBP and randomized to the study agent (IV acetaminophen) or placebo.

Study Timeline

• Status Verified: 2011-10
• Study Start: 2011-10
• Study First Submitted: 2011-10-19
• Study First Submitted QC: 2011-10-26
• Last Update Submitted: 2011-10-26
• Study First Posted: 2011-10-27
• Last Update Posted: 2011-10-27
• Primary Completion: 2012-10

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 85

Inclusion Criteria

• patients who are scheduled to undergo laparoscopic Roux-en-Y gastric bypass surgery (LRYGBP) under general anesthesia.
• age 18 to 65 years
• BMI >35
• ASA scores 1,2, or 3
• a negative pregnancy test for female subjects of childbearing age
• ability to read, understand and provide informed consent to the study procedures
• ability to read and understand the use of pain and nausea scales (VAS)

Exclusion Criteria

• known hypersensitivity to acetaminophen or opioids
• use of opioid or schedule II medications prior to commencement of the study >7 days
• those with chronic pain conditions or significant medical disease requiring pain control
• abnormal liver function (aspartate aminotransferase/alanine aminotransferase/bilirubin > 3X upper limit of normal range, active hepatic disease, clinically significant liver disease, cirrhosis or hepatitis)
• known or suspected alcohol, drug or opiate abuse or dependence; or participation in other clinical study within 30 days of surgery.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
IV acetaminophen	IV acetaminophen	-
IV 0.9% normal saline	IV normal saline	-

Primary Outcome Measures

Name	Time	Method
difference in post-operative opiate consumption (PCA)	hourly, 30 hours from first dose of study agent

Secondary Outcome Measures

Name	Time	Method
post-operative subjective pain intensity	every 2 hours, 30 hours from first dose of study agent
post-operative nausea and vomiting (PONV)	every 2 hours, 30 hours from first dose of study agent
time to first post-operative drug administration	up to 30 hours from first dose of study agent
time to return to flatus	up to 30 hours from first dose of study agent
acceptance of rescue medication	up to 30 hours from first dose of study agent
time to first request for rescue medication	up to 30 hours from first dose of study agent
readiness for discharge	up to 72 hours from the first dose of study agent

Trial Locations

Locations (1)

McLaren Regional Medical Center; 🇺🇸 Flint, Michigan, United States