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Clinical Trials/EUCTR2015-001562-26-GB
EUCTR2015-001562-26-GB
Active, not recruiting
Not Applicable

Preemptive paracetamol for postoperative pain: a randomised, double blind two way crossover trial - Preemptive paracetamol for postoperative pain

niversity of Nottingham0 sitesMay 27, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Nottingham
Status
Active, not recruiting
Last Updated
10 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 27, 2015
End Date
TBD
Last Updated
10 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
niversity of Nottingham

Eligibility Criteria

Inclusion Criteria

  • Age 18\-80 years old
  • Elective non\-malignant cervical spinal surgery
  • Capacity to give informed consent
  • Ability to use PCA device and pain score scale
  • ASA I, II and III
  • General anaesthesia
  • \>50kg in weight
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1\.2 Adults (18\-64 years) yes

Exclusion Criteria

  • Allergy or sensitivity to paracetamol, proparacetamol or morphine
  • Liver disease
  • Renal disease (creatinine clearance \<30ml/min)
  • Bleeding disorder
  • Chronic alcoholism
  • Chronic malnutrition
  • Dehydration
  • G6PD deficiency
  • Hypernatraemia (Na \>150\)
  • Hypokalaemia (K \<3\.5\) and hyperchloraemia

Outcomes

Primary Outcomes

Not specified

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