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QTc-prolongation in the use of antidepressants for anxiety-disorders

QTc-prolongation in the use of antidepressants for anxiety-disorders - QT-prolongation in AD use in Anxietydisorders (QADA)

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38604
Enrollment
60
Registered
2014-07-02
Start date
2014-07-07
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

Long QT syndrome LQTS

Interventions

None listed

Sponsors

Parnassia (Den Haag)
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Age between 18 and 55 years. - Under treatment of the department of Anxiety Disorders, PsyQ, The Hague. - Indication to start with antidepressant medication and not known to have a contra-indication to start with this kind of medication, e.g. severe liver dysfunction, long QT-syndrome, recent myocardial infarct. - Able and willing to give informed consent.

Exclusion criteria

Exclusion criteria: - Patients who had used already antidepressant medication in the 6 weeks prior to the inclusion. - Patients who already use QT-prolonging anti-arrhythmic medication (e.g. sotalol, amiodarone). - Patients who do not meet inclusion-criteria.

Design outcomes

Primary

MeasureTime frame
The main study parameter is the incidence of QTc-prolongation caused by different types of antidepressants use, measured by the difference in QTc-time between baseline and after six weeks of antidepressant use within one person.

Secondary

MeasureTime frame
We investigate whether there is a difference between the different types of antidepressants (serotonin-reuptake inhibitors, serotonine-noradrenaline reuptake inhibitors, tricyclic antidepressants, mono-amine oxidase inhibitors) on the prolongation of the QTc-interval. In addition we will investigate if there are specific risk factors that contribute to this prolongation.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)