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Comparison the efficacy of a combinatory product based on Echium amoenum with Citalopram in Major depressive disorder.

Comparison the efficacy of a combinatory product based on Echium amoenum with Citalopram in Major depressive disorder.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015122725710N1
Enrollment
50
Registered
2016-01-25
Start date
2016-01-20
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

Depression. Mild depressive episode, Moderate depressive episode

Interventions

Intervention 1: Intervention group 1: One citalopram pill with 20 miligram dose every day. Intervention 2: Intervention group 2: Combinatory product based on Echium amoenum in syrup form with 30 milil
Treatment - Drugs
Intervention group 1: One citalopram pill with 20 miligram dose every day
Intervention group 2: Combinatory product based on Echium amoenum in syrup form with 30 mililitre dose per day, two times a day

Sponsors

Vice Chancellor for research of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients are enrolled with age more than 18 years and major depression based on DSM-5 criteria. Exclusion criteria: Depression with psychotic symptoms; Having a history of bipolar disorder; Having suicidal thoughts and any plans to do so; People with a history of recent emotional trauma; Patient dependence on chemical antidepressants; Pregnant and lactating women; Sensitivity to the citalopram; Sensitivity to herbal components of combinatory product; Addiction to alcohol and narcotics

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Depression. Timepoint: Every 4 weeks. Method of measurement: Hamilton Depression Rating Scale.

Primary

MeasureTime frame
Sleep. Timepoint: Every 4 weeks. Method of measurement: Clinical interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mahdi Eslami

Mashhad University of Medical Sciences

eslamim3@mums.ac.ir+98 51 3853 6780

Outcome results

None listed

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