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Comparative study between SSRI and SNRI treatment on depressive patients with Parkinson diseases

Comparative study between SSRI and SNRI treatment on depressive patients with Parkinson diseases - REBORN STUDY(CompaRativE study Between SSRI and SNRI treatment On depRessive patients with ParkinsoN diseases)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015559
Enrollment
40
Registered
2014-10-29
Start date
2014-04-14
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

Parkinson&#39

Interventions

paroxetine 20mg Escitalopram 10mg Duloxetine 40mg

Sponsors

Osaka Redcross Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient should be diagnosed with Parkinson's disease whose score of QIDS-J is 6 and more. 2. The agreement of the study from the applicant is needed. 3. The patient should be 40 years and more.

Exclusion criteria

Exclusion criteria: . have a history of drug already . have a medication with MAO-B inhibitor within 2 weeks before entry. . Taking the medication with Pimozide . Prolonged QT syndrome . severe liver dysfuncation . severe renal dysfunction . poorly controlled obstructive glaucoma . have a history of suicide attempt . Psychiatric disease needed for medication within 1 year

Design outcomes

Primary

MeasureTime frame
The clinical symptoms is evaluated at 6weeks and 10weeks after the drug administration by the following modalities; Primary outcomes 1. Quick Inventory of Depressive Symptomatology: QIDS-J 2. Apathy Score

Secondary

MeasureTime frame
Key secondary outcomes 1. Freezing of Gait Questionnaire:FOG-Q 2. Clinical Global Impression of Severity:CGI-S

Countries

Japan

Contacts

Public ContactMakio Takahashi

Osaka Redcross Hospital, Japan Redcross Neurology

ta@kuhp.kyoto-u.ac.jp06-6774-5111

Outcome results

None listed

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