drugset / Trial / NCT02327013
Investigating the Effect of Vortioxetine in Adult ADHD Patients
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose is to determine the effect of vortioxetine treatment on ADHD symptoms in adult patients with ADHD in a 12 weeks study.
Timeline
- Start
- 2014-12
- Primary completion
- 2016-09
- Completion
- 2016-09
Outcome
Missed primary endpoint
registry analysis (superiority test); Placebo, Combined vs Vortioxetine 10mg, Combined; p = 0.9723; Mean Difference (Final Values) -0.1 (95% CI -3.6 to 3.5); weighed z-score NCT02327013 ↗
registry analysis (superiority test); Placebo, Combined vs Vortioxetine 20mg, Combined; p = 0.6010; Mean Difference (Final Values) 1.0 (95% CI -2.8 to 4.8); weighed z-score NCT02327013 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vortioxetine | Unknown | 10 mg | Oral |
| Subject | Vortioxetine | Unknown | 20 mg | Oral |