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Assessment the effect of chamomilla on early menopausal complications in menopausal women

the effect of chamomilla on early menopausal complications in menopausal women: (A double blind randomized controlled trial)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138902203902N1
Enrollment
100
Registered
2011-03-06
Start date
2011-03-20
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

menopause complication. Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group: 4 100mg-caps of chamomilla, daily for 12 weeks. Intervention 2: Control group: 4 caps of placebo, daily for 12 weeks.
Treatment - Drugs
Placebo
Intervention group: 4 100mg-caps of chamomilla, daily for 12 weeks
Control group: 4 caps of placebo, daily for 12 weeks

Sponsors

Babol university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
47 Years to 62 Years

Inclusion criteria

Inclusion criteria: nclusion criteria: A total score of more than 15 (means that the women needs a hormone replacement therapy), normal pelvic ultrasound or normal pelvic exam , and FSH>40 or two years of lmp. Exclusion criteria: Women who received hormone therapy during the last 6 months, on a diet or herbal treatment; hypercholesterolemia, thyroid disorders, hypertension, diabetes, family history of heart disease, cigarette smoking, serious illnesses (malignancy)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduce of menopause complications. Timepoint: 4 & 8 &12 weeks later. Method of measurement: Scorecard Scale.

Secondary

MeasureTime frame
Enjoyed life. Timepoint: 4&8&12weeks later. Method of measurement: Scorecard Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla Yazdani

Babol university of medical sciences

mohsenzadh2008@gmail.com+98 11 1219 9595

Outcome results

None listed

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