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Thrombogenesis in antipsychotics

Thrombogenesis in antipsychotics - Thrombogenesis in antipsychotics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37658
Enrollment
20
Registered
2012-02-14
Start date
2013-01-24
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

use of antipsychotics use of neuroleptics

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age above 65 years start of an antipsychotic drug informed consent

Exclusion criteria

Exclusion criteria: history of venous tromboemoblism or deep venous thrombosis malignancy with treatment in the last 6 months or palliative treatment bedridden or immobilisation for more than tree days operation in the four previous weeks delirium or acute psychosis, as indication of use of antipsychotic drug use of an antipsychotic in the 6 months previous to the start of the studie other changes in medication within the 10 days of observation

Design outcomes

Primary

MeasureTime frame
1. Platelet activation tests 2. D-dimeer 3. Von Willebrand Factor 4. Osteoprotegerine (OPG)

Secondary

MeasureTime frame
Age (in years) Sexe (male/female) Comorbidity In case of dementia, also the seriousness of the dementia according to the Clinical Dementia Rating scale In case of Parkinson(ism), also the seriousness according to the Hoehn en Yahr criteria Medication Type antipsychotic Dosage of the antipsychotic Indication of prescribing the antipsychotic medication The medical record will be used as the source for the secundairy study parameters

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)