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Effect of oral Royal jelly on menopausal symptoms and sexual function

Effect of oral Royal jelly on menopausal symptoms and sexual function in 50-60 years old menopausal women

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201306022172N14
Enrollment
110
Registered
2013-06-12
Start date
2013-08-23
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

sexual disfunctions , menopause symptems, Symptoms of Menopause. Other sexual dysfunction, not caused by organic disorder or disease,

Interventions

Control group: Placebo Capsules, 100 Mg capsules once daily in tow month
Intervention 1: Intervention group: Royal Jelly Capsules, 100 Mg capsules once daily in tow month. Intervention 2: Control group: Placebo Capsules, 100 Mg capsules once daily in tow month.
Treatment - Other
Placebo
Intervention group: Royal Jelly Capsules, 100 Mg capsules once daily in tow month.

Sponsors

Research Institute for Islamic & Complementary Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Not having physical and psychological diseases in women and their spouses, having coitus at least twice in a month, Not using of sedative and hypnotic drugs, HRT and herbal medicines more than once a week, Not allergic to honey consumption and BMI less than 28 kg m . Exclusion criteria: Not having sexual activity during the study, not using the drug under investigation for more than 6 days in a month, using of any hormonal and herbal medication, using of Soy more than one meal per week, starting any vegetarian diet and allergic and not using of Antibiotics or Antacids during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menopausal symptoms score. Timepoint: End of first month of intervention. Method of measurement: Menopause Rating Scale (MRS) questionnaire.;Sexual function score. Timepoint: End of first month of intervention. Method of measurement: sabbastberg sexual function questionnaire.

Secondary

MeasureTime frame
Sexual function score. Timepoint: End of first and second month of intervention. Method of measurement: sabbastberg sexual function questionnaire.;Menopausal symptoms score. Timepoint: End of first and second month of intervention. Method of measurement: Menopause Rating Scale (MRS) questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsimin Taavoni

Nursing and Midwifery Faculty, tehran University of Medical Sciences

staavoni14@yahoo.com+98 21 6692 1228

Outcome results

None listed

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