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Effect of soybean and fish liver oil on control of hot flashes, sexual disorders and sleep disorders

The effect of Soybean and Fish oil tablets on control of hot flash, sexual and sleep disorders in pre-menopausal and menopausal women 45-64 years old

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200222046584N1
Enrollment
159
Registered
2020-03-19
Start date
2018-10-02
Completion date
Unknown
Last updated
2020-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menopause. Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group one: Patients receive soy pills. Intervention 2: Intervention group: Patients receive fish liver oil pills. Intervention 3: Control group: They dont receive any drug

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 64 Years

Inclusion criteria

Inclusion criteria: Ages between 45 and 64 years Not allergic to soy and fish liver pills Having informed consent for inclusion

Exclusion criteria

Exclusion criteria: Lack of reading and writing skills and unable to answer questions No phone calls to follow up Having a history of more than 10 years of menopause Concomitant use of sulfanamides, methotrexate, triamethrenone, sulfasalazine, estrogen, phenytoin, anti-anxiety and antidepressants, daily chemicals and multivitamins, aspirin and painkillers Hormone therapy and OCP use over the past 3 months Use of complementary herbs to remove vasomotor symptoms over the past month Contraindications to hormone therapy include suspected or diagnosed cancer

Design outcomes

Primary

MeasureTime frame
Comparison of the effect of soy tablets and fish liver oil on TSH level. Timepoint: Before and after the intervention. Method of measurement: TSH measurement in blood.;Comparison of the effect of soy and liver oil pill on lipid profile. Timepoint: Before and after the intervention. Method of measurement: lipid profile measurement in blood.;Measuring the number of hot flashes. Timepoint: Before and after the intervention. Method of measurement: Patient MRS questionnaire.;Measuring the number of times a patient wakes up. Timepoint: Before and after the intervention. Method of measurement: Patient MRS questionnaire.;Patient's sexual reluctance. Timepoint: Before and after the intervention. Method of measurement: Patient MRS questionnaire.;Vaginal dryness. Timepoint: Before and after the intervention. Method of measurement: Patient MRS questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahareh Pourzand

Iran University of Medical Sciences

bahareh.purzand@yahoo.com+98 21 8670 2503

Outcome results

None listed

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