Skip to content

Antidepressant Effect of Asperguo procumbens L. in Comparison with Fluoxetin: a randomized double blind clinical trial

Antidepressant Effect of Asperguo procumbens L. in Comparison with Fluoxetin: a randomized double blind clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138709051457N2
Enrollment
30
Registered
2010-11-02
Start date
2005-04-20
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

Major Depressive Disorder. Mild and Moderate Depressive Episode

Interventions

Intervention 1: Fluoxetine, 30 mg, orally, (10 mg capsules tid) for 6 weeks. Intervention 2: 1200 mg dried extract from arial parts of Asperugo Procumbens L (18 mg total flavenoid) (400 mg dried extra
Treatment - Drugs
Fluoxetine, 30 mg, orally, (10 mg capsules tid) for 6 weeks
1200 mg dried extract from arial parts of Asperugo Procumbens L (18 mg total flavenoid) (400 mg dried extract or 6 mg total flavenoid capsules tid) for 6 weeks

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: DSM-IV criteria for major depressive disorder, Hamilton Depression Rating Scale score 18-25, Informed Consent Exclusion criteria: Intelligence quotient (IQ) less than 70, Positive history of bipolar mood disorder (BMD), consumption of psychostimulator agents in last 2 weeks, Serious medical disease, Allergic reaction to A.procumbens L., Psychotic depression, Positive history of suicidal attempt or suicidal intention, Pregnancy, Positive history of cognitive disorder during last year

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: 2 weeks. Method of measurement: Hamilton Depression Rating Scale.

Secondary

MeasureTime frame
Side effects profile. Timepoint: 2 weeks. Method of measurement: Clinical interview and physical examination and checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehran Zarghami

Mazandaran University of Medical Sciences

mzarghami@mazums.ac.ir & mehran.zarghami@gmail.com+98 15 1328 5659

Outcome results

None listed

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