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
| Type | Name | Description |
|---|---|---|
| DRUG | Acetaminophen | Intravenous Acetaminophen 1,000 mg IV |
| DRUG | Placebo | Placebo - 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.