MedTrace Logo

Preemptive Paracetamol for Postoperative Pain

NCT02425254 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2015-12-03

No results posted yet for this study

Summary

The purpose of this study is to test whether a dose of paracetamol given before surgical incision is more effective at reducing postoperative pain and analgesic consumption in cervical spine surgery versus a dose given at the end of surgery.

Conditions

  • Pain
  • Surgical Wound

Interventions

DRUG

Intravenous paracetamol

1000mg intravenous solution for infusion

DRUG

Intravenous saline 0.9%

0.9% sodium chloride in order to ensure double-blinding

Sponsors & Collaborators

  • University of Nottingham

    lead OTHER

Principal Investigators

  • John Williams · University of Nottiongham

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-06-30
Completion
2018-07-31

More Related Trials

Entities

Diseases

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 NCT02425254 on ClinicalTrials.gov