Clinical Trials Directory

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

TypeNameDescription
DRUGIV paracetamol100 gram paracetamol infusion for moderate pain management
DRUGIV 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.