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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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2008-000427-26-GB
Enrollment
Unknown
Registered
2009-05-15
Start date
2009-06-25
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain post wisdom tooth extraction

Interventions

Trade Name: Perfalgan Product Name: Perfalgan Pharmaceutical Form: Intravenous infusion INN or Proposed INN: N-(4-hydroxyphenyl)acetamide CAS Number: 103-90-2 Pharmaceutical form of the placebo: Intra

Sponsors

Queen Victoria Hospital NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion 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

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 drugs 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

Design outcomes

Primary

MeasureTime frame
Main Objective: Does paracetamol given as a tablet give better pain relief than paracetamol given intravenously in patients having wisdom teeth removed?;Secondary Objective: None;Primary end point(s): We will compare the pain scores of patients in the two study arms one hour postoperatively. This will be done in recovery using a visual analogue scale (VAS) pain scoring system.

Countries

United Kingdom

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026