Clinical Trials Directory

Trials / Terminated

TerminatedNCT01527942

Intravenous Acetaminophen Use With Bariatric Surgery on Morbidly Obese Patients

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

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Trinity Health Of New England · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophenIntravenous Acetaminophen 1,000 mg IV
DRUGPlaceboPlacebo - IV administration 0.9% 100 ml Sodium Chloride (NaCl)

Timeline

Start date
2012-03-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2012-02-07
Last updated
2015-12-17
Results posted
2015-12-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01527942. Inclusion in this directory is not an endorsement.