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

NCT03221998 · Status: UNKNOWN · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2017-07-25

No results posted yet for this study

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

Conditions

  • Obesity, Morbid

Interventions

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

Sponsors & Collaborators

  • Soroka University Medical Center

    lead OTHER

Principal Investigators

  • Michael Semionov, MD · Soroka University Medical Center-Department of Anesthesiology

  • Alexander Zlotnic, PhdMD · Soroka University Medical Center-Department of Anesthesiology

  • Yair Binyamin, MD · Soroka University Medical Center-Department of Anesthesiology

  • Yair Yaish Reina, MD · Soroka University Medical Center-Department of Anesthesiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-07-31
Primary Completion
2019-03-31
Completion
2020-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03221998 on ClinicalTrials.gov