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Pharmacokinetics of haloperidol

Pharmacokinetics of haloperidol - Pharmacokinetics of haloperidol

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39461
Enrollment
20
Registered
2012-01-11
Start date
2012-01-30
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

farmacokinetiek van een geneesmiddel/antipsychoticum pharmacokinetics

Interventions

None listed

Sponsors

Jeroen Bosch Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: age >64 years elective operation with spinal anesthesia elevated risk to develop a delirium and prescription of haloperidol during five days pre-operative in a dose of 1mg/dag as regular care mentally competent informed consent

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
concentration haloperidol in serum and liquor Farmacogenetic polymorfisms of the cytochroom P450 enzym CYP2D6

Secondary

MeasureTime frame
age, gender, race, smoking, medication use

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)