Trials / Unknown
UnknownNCT03221998
The Effect of Timing of Intravenous Paracetamol Administration on Post-surgical Pain
The Effect of Timing of Intravenous Paracetamol Administration on Post-surgical Pain and Cytokines Levels Following Laparoscopic Sleeve Gastrectomy
- Status
- Unknown
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 126 (estimated)
- Sponsor
- Soroka University Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Accepted
Summary
This study is designed as a population-based prospective randomized cohort study. A prospective cohort of patients admitted to laparoscopic sleeve gastrectomy due to morbid obesity
Detailed description
All adult consecutive patients admitted to surgical departments for laparoscopic sleeve gastrectomy will be enrolled prospectively. For the purposes of the current study we want to determine how much paracetamol (acetaminophen) can reduce the cytokines levels in these patients The study enrollment period is planned to be a year. The follow-up period for each patient will be until discharge from the hospital.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | IV paracetamol | 100 gram paracetamol infusion for moderate pain management |
| DRUG | IV saline (NaCl 0.9 %) | 100 ml of Normal Saline (IV NaCl 0.9 %) as placebo |
Timeline
- Start date
- 2017-07-01
- Primary completion
- 2019-03-01
- Completion
- 2020-03-01
- First posted
- 2017-07-19
- Last updated
- 2017-07-25
Source: ClinicalTrials.gov record NCT03221998. Inclusion in this directory is not an endorsement.