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L-carnosine in treatment of major depressive disorder

L-carnosine as an adjuvant in treatment of major depressive disorder : a randomized double-blind study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170123032145N2
Enrollment
50
Registered
2018-04-13
Start date
2018-04-03
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Major Depressive Disorder. Major depressive disorder, single episode

Interventions

Intervention 1: Intervention group: Citalopram tab (max. dose 20mg/day) plus L-carnosine tab 400 mg/ twice per day) for 6 weeks. Intervention 2: Control group: Citalopram tab (max. dose 20mg/day) plus

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients who meet DSM-IV-TR criterion for MDD They should be 18-60 years old and They achieve more than 18 for Hamilton Depression Scale (HamD) Sign consent form

Exclusion criteria

Exclusion criteria: Substance abuse except Nicotine for 1 year before enterance Treated by any anti-depressant medication for 1 month ago Treated by ECT for 2 months ago Presence of psychotic feature Previous diagnosed as Bipolar patient Suicidal thoughts They will evaluate for thyroid, cardiac, liver, kidney diseases, or any medical cause for depression, pregnancy, lactation before entrance and any mentioned conditions will cause exclusion from study.

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Scale score. Timepoint: 0, 2, 4, 6 weeks. Method of measurement: Hamilton Depression Scale.

Secondary

MeasureTime frame
Side effects. Timepoint: 1,2,4,6 weeks. Method of measurement: side effects checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammadreza Shalbafan

Iran University of Medical Sciences

shalbafan.mr@iums.ac.ir+98 21 4452 5615

Outcome results

None listed

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