EUCTR2006-002208-32-GB
Active, not recruiting
Not Applicable
A comparison of the analgesic efficacy of oral and intravenous paracetamol (perfalgan) in a day case setting - Oral versus IV paracetamol
York Hospital NHS Trust0 sitesSeptember 18, 2006
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- York Hospital NHS Trust
- Status
- Active, not recruiting
- Last Updated
- 14 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All patients on the list for day case knee arthroscopy aged between 18 to 60 years and weighing between 50 to 90 kg will be eligible for the study.
- •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) no
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Age \<18 and \>60 years, ASA 3 or 4 (American society of anaestesiologist classification \- ASA 3 \& 4 are sicker patients than ASA 1 \& 2\), known allergy to paracetamol, patients who had paracetamol in the last 12 hours, pregnant or breast feeding women, history of complete non\-responsiveness to acetaminophen, inflammatory bowel disease, chronic pain patients, arthroscopies related to infection (where surgeon would not instil local anaesthetic), bilateral arthroscopies.
Outcomes
Primary Outcomes
Not specified
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