Skip to content

The comparison of the effect of fenugreek seed, Flaxseed and soy on hot flashes menopause.

The comparison of the effect of fenugreek seed, Flaxseed and soy on hot flashes menopause.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138807122545N1
Enrollment
120
Registered
2011-07-24
Start date
2008-07-20
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

Menopausal hot flash. Menopausal and other perimenopausal disorders

Interventions

Intervention 1: Fenugreek seed group (6g daily) for 4 weeks consequently. Intervention 2: Flaxseed group (25 g daily )for 4 weeks consequently. Intervention 3: Soy group ( 25 g daily )for 4 weeks co
Treatment - Drugs
Placebo
Fenugreek seed group (6g daily) for 4 weeks consequently
Flaxseed group (25 g daily )for 4 weeks consequently.
Soy group ( 25 g daily )for 4 weeks consequently
Wheat group (25 g daily ) for 4 weeks consequently

Sponsors

Vice chancellor for research, Arak University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: Women with amenorrhea during the previous 12 months with reporting menopausal hot flash , normal blood pressure without use of estrogen and progesterone, anti depressant and anti anxiety drugs during the previous 6 months as well as with out use of anticoagulants and NSAIDs for example ibuprofen and with out history of asthma and allergy will include in the research. Women with incorrect use of herbal plants, home change and skin irritation will exclude from study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency of hot flash. Timepoint: Initial of intervention and 4 week and 8 weeks after intervention. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Intensity of hotflashs. Timepoint: initial of study,4 , 8 weeks after intervention. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaimeh Akbari Torkestani

Arak University of Medical Sciences , Arak , Iran .

tnaimeh@yahoo.com+98 86 1417 3503

Outcome results

None listed

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