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The Comparison of the Effect of Omega3 and Folic Acid Oral Tablet on Hot Flashes in Menopausal Women

The Comparison of the Effect of Omega3 and Folic Acid Oral Tablet on Hot Flashes in Menopausal Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017011131880N1
Enrollment
120
Registered
2017-01-24
Start date
2016-11-21
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. Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group:omega3 1 tablet 1000 mg daily, group folic acid 1 tablet 1 mg daily?omega3 is made zahravi , folic acid made Shahid Beheshti University of Medical Science in the Sc
Placebo
Intervention group:omega3 1 tablet 1000 mg daily, group folic acid 1 tablet 1 mg daily?omega3 is made zahravi , folic acid made Shahid Beheshti University of Medical Science in the School of Pharmacy
Control group: placebo 1 tablet daily for 3 months , made School of Pharmacy Shahid, Beheshti University of Medical Sciences

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 : Iranian, age 45-60 years, menopause is the normal type have,reporting at least two times hot flashes per day , with literacy being studied components or a family member, body mass index 20 to 30, non receiving hormone therapy , anti-depressants or tranquilizers, supplements and herbal medicines, no known underlying disease (hypertension, diabetes, epilepsy, etc.), the lack of experience of such as relatives died in the last 6 months of stress, separation of spouses and absence of estrogen-dependent cancer, non consumption of more than 2 servings of fish per weeks, insensitivity to fish or fish oil, seafood, avoiding the use of any drugs to improve the symptoms of hot flashes, at least one year and a maximum of three years have menstruation, exercise not more than 2 times a week for 20-30Dqyqh,Exclusion criteria: the other drug use during the study, in case of complications or allergic drugs (omega-3 or folic acid), identifying any physical or mental illness during the study, lack of proper use of drugs or placebo over three days

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The severity of hot flashes. Timepoint: Before the intervention, one month and two months and three months after intervention. Method of measurement: Daily hot flash diary form.

Secondary

MeasureTime frame
Duration of hot flashes. Timepoint: Before the intervention, one month and two months and three months after intervention. Method of measurement: Daily hot flash diary form.;Frequency hot flashes. Timepoint: Before the intervention, one month and two months and three months after intervention. Method of measurement: Daily hot flash diary form.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmasoumeh chamani

Iran University of Medical Sciences, School of Nursing and Midwifery

m66.chamani@gmail.comchamani.m@tak.iums.ac.ir+98 21 8888 2885

Outcome results

None listed

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