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The efficacy of L-carnitine addition in treatment of major depressive disorder

Comparing the efficacy of L-carnitine and sertraline compared with sertraline alone on severity of depression in patients with major depressive disorder: A double blinded randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150630022991N15
Enrollment
60
Registered
2021-02-26
Start date
2021-02-08
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Condition 1: Major depressive disorder. Condition 2: Major depressive disorder. Major depressive disorder, single episode Major depressive disorder, recurrent severe without psychotic features

Interventions

Intervention 1: Intervention group: will receive 1000 milligram of L-carnitine oral capsule daily made by Vana-Darougostar Pharmaceutical Company along with 100 milligram of sertraline made by Tehran-

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of major depressive disorder based on diagnostic and statistical manual of mental disorders, 5th edition (DSM-5) through a psychiatrist clinical interview Age 18 years and over

Exclusion criteria

Exclusion criteria: Previous history of high mood (mania and/ or hypomania) Presence of dementia Cognitive dysfunction Acute psychiatric disorders based on the opinion of a psychiatrist Serious somatic disorders Substance dependence, except cigarettes and caffeine Consumption of drugs that makes the incidence of depression in the patient

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: At baseline, the third and sixth weeks after the treatment. Method of measurement: Based on Beck depression scale.

Secondary

MeasureTime frame
Drug side effects. Timepoint: At baseline, the third and sixth weeks after the treatment. Method of measurement: Medical visit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSussan Moudi, MD

Babol University of Medical Sciences

sussan.mouodi@gmail.com+98 11 3219 7667

Outcome results

None listed

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