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Investigation for the effect of duloxetine on adolescent depression; Ver. 2

Investigation for the effect of duloxetine on adolescent depression; Ver. 2 - E-DAD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016192
Enrollment
100
Registered
2015-03-01
Start date
2015-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Interventions

* On
y cognitive behavioral therapy of 50 minutes. * 1W, 4W, 6W, 8W total 4 times. * Cognitive behavioral therapy of 50 min. and duloxetine. * CBT
1W, 4W, 6W, 8W total 4 times. * Duloxetine
At first we will prescribe 20mg. 1 week later we will increase to 40mg. 3 week later, depending on the request of subjects, we will regulate quantity of prescription from 20mg to 60mg. We will not cha

Sponsors

Shiga University of Medical Science
Lead Sponsor
Japanese Red Cross Society Nagahama Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients of Major Depressive Disorder diagnosed by both of DSM-IV-TR and DSM-5.

Exclusion criteria

Exclusion criteria: * Remitted or partial remitted patients * Patients with sever inhibition so as not to tolerate CBT, questionnaire and structured interview * Pregnant women * Patients with physical disorder

Design outcomes

Primary

MeasureTime frame
Quolity of Life; SF-36v2

Secondary

MeasureTime frame
Depression; BDI-II Anxiety; STAI Autistic Tnedency; PARS-TR Attention Deficit and/or Hyperactivity; ADHD-RS

Countries

Japan

Contacts

Public ContactTakahiko Inagaki

Shiga University of Medical Science Department of Community Psychiatric Medicine

kerosuke@belle.shiga-med.ac.jp077-548-2291

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026