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Clinical Trial Summary

Observational study in 6 psychiatric hospitals in Flanders. Patients are included when a QT-prolonging drug is added to a medication profile that already contains a potential QT-prolonging drug. An ECG is taken before the administration of the new drug and a week after starting the new drug to investigate the change in duration of the QTc-interval. Risk factors for developing QT-prolongation and blood concentrations of potassium and creatinine are documented.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02043925
Study type Observational
Source Katholieke Universiteit Leuven
Contact
Status Completed
Phase N/A
Start date October 2010
Completion date March 2015

See also
  Status Clinical Trial Phase
Completed NCT02043912 - Drug Interactions With Risk of QT-prolongation in a General Hospital N/A
Completed NCT02068170 - Risk of QT-prolongation and Torsade de Pointes in Patients Treated With Acute Medication in a University Hospital N/A