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Efficacy and tolerability of escitalopram versus paroxetine-CR in Japanese patients with major depressive disorder: a randomized, masked-rater trial

Efficacy and tolerability of escitalopram versus paroxetine-CR in Japanese patients with major depressive disorder: a randomized, masked-rater trial - A randomized controlled trial of escitalopram versus paroxetine-CR in major depressive disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011191
Enrollment
200
Registered
2013-07-16
Start date
2013-07-16
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

Escitalopram Paroxetine-CR

Sponsors

Department of Psychiatry, Fujita Health University School of Medicine
Lead Sponsor
The Okehazama Hospital The Jindai Hospital The St. Cross Hospital The Toyota Memorial Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients (inpatients and outpatients), diagnosed with major depressive disorder (according to the DSM-IV-TR criteria) Patients with HAM-D17 total score 20 or more

Exclusion criteria

Exclusion criteria: Patient with the following disorders (based on DSM-IV-TR criteria): psychotic disorders, pervasive developmental disorders, bipolar disorder, obsessive-compulsive disorder, Axis-2 disorder. Patients with substance abuse or dependence (excluding nicotine and caffeine) meeting DSM-IV-TR criteria Patients taking MAO inhibitors with in14 days (or Patients treated with MAO inhibitors within 14 days) Patients taking pimozide Patients with allergies to escitalopram, citalopram and paroxetine Patients with QT interval prolongation Patients treated with ECT within the previous 6 months Patients having severe physical disease Patients who are pregnant or may become pregnant Patients at significant risk of suicide (having a score >3 on HAM-D item 11) Patients who had made suicide attempt within the past year

Design outcomes

Primary

MeasureTime frame
The Hamilton Rating Scale for Depression

Secondary

MeasureTime frame
Remission rate

Countries

Japan

Contacts

Public ContactTaro Kishi

Fujita Health University School of Medicine Department of Psychiatry

tarok@fujita-hu.ac.jp0562939250

Outcome results

None listed

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