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Descriptive Toxicogenomics of paracetamol in humans

Descriptive Toxicogenomics of paracetamol in humans - Toxicogenomics of paracetamol

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON35449
Enrollment
30
Registered
2009-02-24
Start date
2009-06-22
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

liver resection partial chirugical removal of the liver

Interventions

An intervention is only applicable to study group 3-5, healthy volunteers, receiving a low dose of 2 gram APAP (4*0.5 gram APAP over 24 hours). In study group 1 and 2, the administration of 4 grams

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For liver / pancreas resection patients: •All patients undergoing a non laparoscopic liver or pancreas resection. •Age above 18 years For healthy volunteers: •Age match to liver / colon resection group

Exclusion criteria

Exclusion criteria: •Alcohol abuse up to 6 months before participation in this research. •Aberrations or insufficiency of kidney, liver, gut, heart or longs apart from the disease to be treated. •Presence of persistent inflammation in the gut or liver. •Use of drug known to affect the liver metabolism. •Endocrine or metabolic aberrations. •Anaemia or infection. •HIV infection or hepatitis.

Design outcomes

Primary

MeasureTime frame
The main study parameters are changes in gene expression profile and metabolomic profile measured after and caused by APAP exposure.

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)