Paracetamol CSF Pharmacokinetics Study

Barts & The London NHS Trust

Status and phase: Completed; Phase 4

Conditions: Paracetamol

Treatments: Drug: Administration of paracetamol

Study type: Interventional

Funder types: Other

Identifiers

NCT01821872

7258 (Other Identifier)

Details and patient eligibility

About

Despite its use for decades all over the world, the exact mechanism of action of paracetamol is not fully understood and essentially involves a combination of hypotheses. It is known to have an effect via the central nervous system, and of the many mechanisms proposed, one hypothesis is that it may have indirectly activate CB1 (cannabinoid) receptors, through its novel metabolite AM404.

This study aims to elucidate cerebrospinal levels of paracetamol and to measure the concentration of its metabolites, including AM404 in CSF. This may, in turn, give us useful information on the mechanism of action of paracetamol.

Full description

Patients undergoing spinal blockade for urological surgery were administered 1g paracetamol intravenously at varying intervals prior to spinal anaesthesia, at which time 5mls of cerebrospinal fluid and 10mls of blood were sampled, and analysed for concentrations of paracetamol, paracetamol glucuronide, paracetamol sulphate, and AM404, a known endocannabinoid reuptake inhibitor, and metabolite of paracetamol.

Paracetamol readily penetrates into the cerebrospinal fluid in animal studies and in children. This could account for the rapid central analgesic and antipyretic action of intravenous paracetamol however this remains to be studied in adults. AM404 has never before been identified in humans, and its presence in CSF following paracetamol supports the hypothesis of a central mechanism of action of paracetamol via AM404.

Enrollment: 30 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult subjects aged 18 to 80 years
• Subjects undergoing surgery who require a spinal anaesthetic and paracetamol as part of their routine anaesthetic plan
• Subjects with an American Society of Anesthesiology score of I-III

Exclusion criteria

• Subjects with any contraindication to spinal anaesthesia
• Subjects with known clotting abnormalities
• Pregnant or lactating women
• Subjects with known hypersensitivity to paracetamol
• Patients with severe hepatocellular insufficiency
• Patients already taking regular doses of paracetamol
• Any subjects deemed medically unsuitable by the investigator

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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30 participants in 3 patient groups

Sampling at approx 15 minutes

Active Comparator group

Description:

Plasma and CSF samples to be taken at 15 minutes post administration of intravenous paracetamol

Treatment:

Drug: Administration of paracetamol

Sampling at approx 30 minutes

Active Comparator group

Description:

Plasma and CSF samples to be taken at 30 minutes post administration of intravenous paracetamol

Treatment:

Drug: Administration of paracetamol

Sampling at approx 120minutes

Active Comparator group

Description:

Plasma and CSF samples to be taken at 120 minutes post administration of intravenous paracetamol

Treatment:

Drug: Administration of paracetamol