EUCTR2010-019488-12-GBActive, not recruitingNot Applicable
A Single Centre Prospective Randomised Study to Investigate the Metabolism of Intravenous Paracetamol in Humans - Paracetamol CSF Study Version 1
Joint Research Office, Barts and The London NHS Trust0 sitesStarted: November 9, 2010Last updated:
Conditions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •Adult patients aged 18 and 80 years from whom full written informed consent will be sought.
- •Patients undergoing surgery who require a spinal anaesthetic and paracetamol as part of their routine anaesthetic
- •Patients who fall into the American Society of Anesthesiologists scoring system of ASA I-III.
- •Patients with no known clotting abnormalities
- •Patients who have given written informed consent
- •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
- •Patients with any contraindication to spinal anaesthesia
- •Patients with known clotting abnormalities.
- •Pregnant women.
- •Patients who have known hypersensitivity to paracetamol.
- •Any patients who are deemed unsuitable by the investigators due to medical reasons.
- •Subjects who have received an investigational drug or have used an investigational device in the 30 days preceding to study entry.
Investigators
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