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The effect of Citicoline in major depression

Citichholine as adjuvant therapy in major depression: a randomized and double blind study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201502191556N74
Enrollment
50
Registered
2015-08-29
Start date
2015-09-23
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 depression. Major Depressive episode

Interventions

Intervention 1: Citalopram 40 mg /day plus capsule citicolin 100 mg BID as the main drug for six weeks as the intervention group. Intervention 2: Citalopram 40 mg/day plus Placebo for six weeks as th
Treatment - Drugs
Placebo
Citalopram 40 mg /day plus capsule citicolin 100 mg BID as the main drug for six weeks as the intervention group
Citalopram 40 mg/day plus Placebo for six weeks as the control group

Sponsors

Tehran Medical Sciences University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: aInclusion criteria: age between 18 – 50 years old; diagnoses are done on the basis of Diagnostic & Statistical Mental Disorders (DSMD); HRSD score above14; signing informed consent. Exclusion criteria: demise of a close relative; having other psychocognitive affliction; taking antidepressive & psychoactive drugs within the last two months; heart complication; thyroid complication; history of ECT (Electroconvulsive Therapy); alcohol & drug addiction; reaching menopause age; pregnancy and lactation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Assessment in first and on 2th, 4th and 6th weeks after onset of receiving medication. Method of measurement: Measurment by HAMD.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shahin Akhondzadeh

Tehran University of Medical Sciences

sakhond@yahoo.com+98 21 5541 2222

Outcome results

None listed

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