Skip to content

Effectiveness of Vitagnus on depression and menopausal signs in climactric women

Comparison Serteralin and combination of Vitagnus and sertraline on depression and menopausal signs in climactric women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016041322991N4
Enrollment
40
Registered
2016-04-23
Start date
2016-04-08
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

Menopausal and other perimenopausal disorders. Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group: Sertraline (50-200 milligram per day) besides vitagnus (one tablet a day) for six weeks. Intervention 2: Control group: Sertraline (in the dose of 50-200 milligram
Treatment - Drugs
Intervention group: Sertraline (50-200 milligram per day) besides vitagnus (one tablet a day) for six weeks
Control group: Sertraline (in the dose of 50-200 milligram per day)

Sponsors

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

Eligibility

Sex/Gender
Female
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The patients who have been menopaused at least two years ago; Depression (the score more than 16 in Beck Depression Scale); The patient´s desire to participate in the study Exclusion criteria: The history of elevated mood; Psychosis; Severe suicidal thoughts; The history of renal disorders; The history of hepatic disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patient´s depressive condition. Timepoint: 3th and 6th weeks after treatment. Method of measurement: Beck Depression Scale.;Menopausal signs. Timepoint: 3th and 6th weeks after treatment. Method of measurement: Menopausal Rating Scale (Kapperman Scale).

Secondary

MeasureTime frame
Adverse drug reaction. Timepoint: 3rd and 6th weeks after treatment. Method of measurement: Interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSussan Moudi, MD

Babol University of Medical Sciences

sussan.mouodi@gmail.com+98 11 3219 0624

Outcome results

None listed

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