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Riluzole in the treatment of major depression

Riluzole as adjuvant therapy in the treatment o moderate to severe major depression: A double - blind placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201307181556N54
Enrollment
40
Registered
2013-07-18
Start date
2013-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Major Depressive episode. Major Depressive episode

Interventions

Intervention 1: Tablet Citalopram 40 mg/day plus Tablet Riluzole 50 mg twice per day as intervention group for 6 weeks. Intervention 2: Tablet Citalopram 40 mg/day plus Tablet placebo as control group
Treatment - Drugs
Placebo
Tablet Citalopram 40 mg/day plus Tablet Riluzole 50 mg twice per day as intervention group for 6 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:1. Presence of Major Depressive Disorder based on DSM-IV criteria; Baseline Hamilton Depression Rating Scale (HAM-D) (17-item) score of at least 19. Exclusion criteria: 1. Presence of Psychosis;2.any other diagnosis in Axis I and II; 3.Receiving psychotropic medications;4.receiving any antidepressants during past one month or ECT during past two months;5. Presence of hypothyroidism;6. cardiovascular problems; 7. pregnancy or nursing women; 8.7-rising liver transaminases to three times the upper limit of normal or higher

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Baseline and weeks 2,4 and 6. Method of measurement: Hamiltion Depression Rating Scale 17-Item.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactProf. Shahin Akhondzadeh

Tehran University of Medical Sciences

S.akhond@sina.tums.ac.ir+98 21 5541 2222

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026