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Clinical Trials/EUCTR2008-000427-26-GB
EUCTR2008-000427-26-GB
Active, not recruiting
Not Applicable

A Comparison of Pre-Medication with Oral Paracetamol versus Intravenous Paracetamol Given at Time of Induction for Postoperative Analgesia Following Wisdom Tooth Extraction - Oral vs IV Paracetamol for Wisdom Tooth Extractions

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain post wisdom tooth extraction
Sponsor
Queen Victoria Hospital NHS Foundation Trust
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 15, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients over 18 having a general anaesthetic for wisdom teeth extractions – at least one of them being a lower tooth.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • o Patients who are unable to give full consent, or who do not wish to take part in the trial
  • o Hypersensitivity or history of serious adverse reactions to paracetamol or Non\-Steroidal Anti Inflammatory
  • o Active liver disease
  • o Renal Dysfunction
  • o Pregnant or breast feeding women
  • o Alcohol or drug abuse
  • o History of unresponsiveness to paracetamol
  • o Gastric or Peptic ulcer disease
  • o Inflammatory bowel disease
  • o Blood coagulation abnormalities

Outcomes

Primary Outcomes

Not specified

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