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Therapeutic effect of herbal formulation Hypericum perforatum with antidepressant drug

A comparison of tricyclic antidepressant augmentation with herbal formation Hypericum perforatum and placebo in depressed outpatients referred to psychiatric clinic and Golestan hospital / Ahvaz /Iran

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201010124917N1
Enrollment
40
Registered
2011-01-20
Start date
2010-07-23
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

Condition 1: Moderate depression. Condition 2: Mild depression. Moderate depressive episode Mild depressive episode

Interventions

Intervention 1: Tricyclic antidepressant with average dose, as well as Hypericum Perforatum (a herbal formulation), three times a day 6 weeks. Intervention 2: Tricyclic antidepressant with average dos
Treatment - Drugs
Placebo
Tricyclic antidepressant with average dose, as well as Hypericum Perforatum (a herbal formulation), three times a day 6 weeks
Tricyclic antidepressant with average dose, as well as placebo, three times a day 6 weeks

Sponsors

Vice-chancellor for Research, Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Major depressive disorder diagnosed by a psychiatrist based on DSM-IV-TR criteria, age range between 18-55 years, filling the consent form, mild or moderate severity of depression Exclusion Criteria: Pregnancy, breast feeding, organic or neurological disorder featuring both clinically, Axis II psychiatric disorder, presence of simultaneous psychiatric disorder diagnosis in axis I, using alcohol and other addictive substances other than nicotine and caffeine in a one-month past, exacerbation of symptoms of severe depression or psychotic disorders, Signs that require hospitalization and emergency action such as suicidal thoughts and behaviors, Not receiving ECT over three months prior to the study, any particular sensitivity to plant grass herbal tea, consumption of medicine such as lithium, anticonvulsants, sumatriptan, Al Biped, serotonin-reuptake inhibitors, buspirone, Argo compounds, Selegiline, stimulants, anti-congestive, contraceptives, cimetidine, theophylline or thyroid hormones during 7 days prior to the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Improvement of sleep. Timepoint: 3 weeks. Method of measurement: clinical interview.;Improvement of apetite. Timepoint: 3 weeks. Method of measurement: clinical interview.

Secondary

MeasureTime frame
Treatment of depression. Timepoint: 3 weeks. Method of measurement: Beck Rating Scale for Depression.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Zhale Nilsaz

Ahvaz Jundishapur University of Medical Sciences

drbabapour@yahoo.com+98 61 1333 8770

Outcome results

None listed

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