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The Effect of Timing of Intravenous Paracetamol Administration on Post-surgical Pain

Obesity, Morbid Clinical Trial

Official title:
The Effect of Timing of Intravenous Paracetamol Administration on Post-surgical Pain and Cytokines Levels Following Laparoscopic Sleeve Gastrectomy

Clinical Trial 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

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03221998
Study type Interventional
Source Soroka University Medical Center
Contact Yair Binyamin, MD
Phone +972586963871
Email Yairben1@gmail.com
Status Not yet recruiting
Phase Early Phase 1
Start date July 2017
Completion date March 2020
View Details
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