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Clinical Trial Summary

In this epidemiological point prevalence study, medication profiles of patients with haloperidol treatment will be checked for drug interactions with risk of QT-prolongation. Additional clinical risk factors for developing QT-prolongation and safety measurements will be documented.


Clinical Trial Description

Study design: epidemiological point prevalence study

Target population: Patients with haloperidol treatment

The following aspects will be investigated:

- The medication profiles will be checked for drug interactions with risk of QT-prolongation.

- Clinical risk factors for developing QT-prolongation (gender, age, (history of) cardiovascular disease, comorbidity,...) and lab results will be collected.

- Safety measurements (e.g. ECG) will be documented. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02043912
Study type Observational
Source Katholieke Universiteit Leuven
Contact
Status Completed
Phase N/A
Start date July 2013
Completion date April 2014

See also
  Status Clinical Trial Phase
Completed NCT02043925 - QT-prolongation in Psychiatric Hospitals N/A
Completed NCT02068170 - Risk of QT-prolongation and Torsade de Pointes in Patients Treated With Acute Medication in a University Hospital N/A