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Soy Isoflavone on hot flushes, endometrial thickness and breast clinical and sonographic

Effect of Soy Isoflavone on hot flushes, endometrial thickness and breast clinical and sonographic features

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100706004329N5
Enrollment
204
Registered
2018-02-06
Start date
2015-05-01
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Hot flash.

Interventions

Intervention 1: Intervention group: received tablet Soyagol ( 50 mg isoflavone) ,Goldaru Pharmaceutical Company , one before lunch and one before dinner, for 12 weeks. Intervention 2: Control group

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: over 40 years of age body mass index in range of 20-35Kg/m2 With hot flushes

Exclusion criteria

Exclusion criteria: Women with previous history of cancer,diabetes mellitus or renal, hepatic, and heart failure or abnormal uterine bleeding, mioma, ovarian cyst, Poly Cystic Ovarian syndrome(PCOS), endometriosis hormone therapy during the last three months, Patients with disability or known history of drug or alcohol consumption Cigarette smoking and caffeine consumption

Design outcomes

Primary

MeasureTime frame
Hot flashing were categorized in mild, moderate and severe. Timepoint: before and 6 and 12 months after intervention. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Endometrial thickness. Timepoint: Before and 6, 12 months after intervention. Method of measurement: Endometrial thickness was evaluated using ulthrasonography.;Breast changes. Timepoint: Before and 6, 12 months after intervention. Method of measurement: Breast sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSadaf Alipour

Tehran University of Medical Sciences

sadafalipour@yahoo.com+98 21 7771 9922

Outcome results

None listed

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