Trials / Unknown
UnknownNCT02154464
Morphine-sparing Effect of Intravenous Paracetamol for Post-operative Pain Management Following Laparoscopic Gastric Banding in Morbidly Obese Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 220 (estimated)
- Sponsor
- Soroka University Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The investigators predict that giving patients paracetamol in the operative period will reduce their need for opioid pain reducers in the post operative setting.
Detailed description
This study is designed as a population-based prospective, double blind cohort study. A prospective cohort of patients admitted to laparoscopic gastric banding due to morbid obesity STUDY GOALS * To evaluate the morphine-sparing effect of paracetamol IV in obese patients undergoing bariatric surgery. * To identify potential ability of paracetamol IV to attenuate or relief postoperative pain in obesity patient undergoing bariatric surgery * To determine effectiveness of paracetamol IV to reduce postoperative complication rate.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Paracetamol | |
| DRUG | Placebo |
Timeline
- Start date
- 2014-06-01
- Primary completion
- 2016-06-01
- First posted
- 2014-06-03
- Last updated
- 2014-06-03
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT02154464. Inclusion in this directory is not an endorsement.