Skip to content

Effect of Cornus mas fruit on menopausal symptoms in menopausal women refers to the Clinics of Rasool Akram Hospital

Effect of Cornus mas fruit on menopausal symptoms in menopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012070210166N1
Enrollment
84
Registered
2012-07-13
Start date
2012-09-22
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 symptoms. Other obstetric conditions, not elsewhere classified

Interventions

The intervention group will receive daily 3 capsules containing 500 mg of powdered Cornus mas for 4 weeks. Placebo group will receive daily 3 capsules containing 500 mg starch powder for 4 weeks..
Treatment - Drugs
The intervention group will receive daily 3 capsules containing 500 mg of powdered Cornus mas for 4 weeks. Placebo group will receive daily 3 capsules containing 500 mg starch powder for 4 weeks.

Sponsors

Vice-chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for intervention: Age 60-45 years; Amenorrhea for at least 12 months; Having at least 3 times in hot flushing medium during 24 hours and at least 2 weeks before study; Lack of history of allergy to Cornus mas use and its products; Not receiving hormone replacement therapy within 6 months; At present not use of estrogen and Medroxyprogestrone; Lack of effective drugs on hot flashes, such as clonidine, methyldopa, , veralpereid, naloxone and Tibolone; Lack of vaginal bleeding of unknown origin; Have not active liver disease and renal failure; No history of malignancy; No history of thromboembolism; Willingness to participate in the study. Exclusion criteria of intervention: Vegetarian diet; Soya consumption; Cornus mas consumption; Regular use of vitamin; Smoking; take antibiotics ; Unwillingness to continue Cornus mas consumption.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menopausal symptoms, some inflammatory and bone markers, body fat percent. Timepoint: Ten days before the intervention- Beginning of the second ten days of study- For ten days in the third and fourth and fifth of the study. Method of measurement: Kupperman menopausal index, Bio-Chemical testing, Bioelectrical Impedance Analysis.

Secondary

MeasureTime frame
Abdominal pain? diarrhea. Timepoint: Once every ten days. Method of measurement: By interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahnaz Rimaz

Iran University of Medical Sciences

sh-rimaz@iums.ac.ir; srimaz2000@yahoo.com+98 21 8860 4645

Outcome results

None listed

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