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View Clinical Trial (Medical Research Study)


Effect of Intravenous Acetaminophen on Postoperative Pain of Morbidly Obese Patients Undergoing Laparoscopic Bariatric Surgery: A Randomized, Placebo-Controlled Trial

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City:   Hartford
State:   Connecticut
Zip Code:   06105
Conditions:   Obesity - Pain
Purpose:   Bariatric patients usually require the use of either intravenous or oral opioid medications. The use of opioids, however, is often associated with side-effects such as nausea, sedation pruritus, urinary retention and respiratory depression with often delay patient discharge. This study makes use of intravenous acetaminophen , a non-opioid analgesic preoperatively to determine if this will decrease the use of opioids post-operatively for pain management in morbidly obese patients undergoing laparoscopic bariatric surgery.
Study Summary:  
Criteria:   Inclusion Criteria: - Morbidly Obese and body mass index (BMI) of 35 - Between ages 20-17 - Candidates for Laparoscopic Bariatric Surgery Exclusion Criteria: - know hypersensitivity to acetaminophen or opioids - impairment in liver function - renal dysfunction - mental retardation
NCT ID:   NCT01527942
Primary Contact:   Principal Investigator
Ioannis Raftopoulos, MD
Saint Francis

Backup Contact:   N/A
Location Contact:   Hartford, Connecticut 06105
United States



There is no listed contact information for this specific location.

Site Status: N/A

Click here to see:
  • Clinical trials for Obesity in Hartford, Connecticut
  • Clinical trials for Pain in Hartford, Connecticut

Data Source:   ClinicalTrials.gov
Date Processed:   May 21, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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