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A better understanding of the response and side effect of clozapine use

Phenomics & Genomics of Clozapine Pharmacotherapy – New Users

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON20290
Enrollment
60
Registered
2015-06-19
Start date
2015-07-01
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Schizophrenia,schizophreniform and schizoaffective disorder Clozapine, psychotic disorders

Interventions

None

Sponsors

University Medical Center Utrecht
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -he/she is about to initiate CLZ (i.e. he/she has an indication to start CLZ treatment according to the treating physician and he/she is willing to start on CLZ) -he/she has received a diagnosis of schizophrenia, schizophreniform disorder, schizoaffective disorder or psychosis not otherwise specified. -his/her age must be ≥18 years old -he/she must be able to speak and read the Dutch language -he/she must be mentally competent with regard to a decision to participate in the current study

Exclusion criteria

Exclusion criteria: - admission to a psychiatric unit involuntarily in the context of an ‘inbewaringstelling’ (IBS) - a history of Parkinson’s disease

Design outcomes

Primary

MeasureTime frame
Reponse and the development of ADRs after clozapine intake. We think this is influenced by methylation patterns and gene expression

Secondary

MeasureTime frame
We measure non-genetic factors such as smoking, cannabis use, duration of illness etc., because we think these influence treatment outcome (ADRs+response) as well. In addition, we use the data with our other protocol (NTR 5257) to create a prediction model for clozapine response and side effects.

Contacts

Public ContactMarte van der Horst

UMCU A01.126

mzvanderhorst@gmail.com0887551460

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)