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Comparison the effect of Echium amoenum extract with fluoxetine on depression in menopausal women.

Comparison the effect of Echium amoenum extract with fluoxetine on depression in menopausal women.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017051133925N1
Enrollment
72
Registered
2017-07-18
Start date
2017-09-23
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

Depression. Recurrent depressive disorder, current episode moderate.Recurrent depressive disorder, current episode severe without psychotic symptoms

Interventions

Intervention 1: In the intervention group 500 mg Echium amoenum extract (capsule) will be administered daily for 8 week . Intervention 2: In The control group 20 mg fluoxetine (capsule) will be admini
Treatment - Drugs
In the intervention group 500 mg Echium amoenum extract (capsule) will be administered daily for 8 week .
In The control group 20 mg fluoxetine (capsule) will be administered daily for 8 weeks .

Sponsors

Vice chancellor for research, Ahvaz Jundishapur University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria require that the menopausal women have amenorrhea for at least 12 months; the participants age be between 45 and 60 years and Major depression criteria based on DSM-5, According to psychiatrist verdict; patients with moderate to severe depression (14-22 with a test of Hamilton depression score). The exclusion criteria include: patients with depression that have suicidal thoughts; severe depression; Sensitivity to the fluoxetine; Getting any systemic disease such as( high blood pressure;diabetes; renal disease); Taking antidepressant medication; alcohol consumption; Use of herbal medicines for treatment of menopausal symptoms; use of Drugs that interfere with fluoxetine; surgery such as hysterectomy radical women, Vaginoplasty and artificial menopause.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression levels. Timepoint: 0 week, 4 week, 6 week, 8 week. Method of measurement: phycologist and Hamilton questioner.

Secondary

MeasureTime frame
Diarrhea. Timepoint: Daily. Method of measurement: Self report.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmitra tadayon najafabady

ahvaz medical university

mitratadayon2000@yahoo.com+98 61 3373 8331

Outcome results

None listed

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