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Investigating the effect of asparagus officinalis on postmenopausal women’s sexual function and severity of menopausal symptoms

Investigating the effect of asparagus officinalis on postmenopausal women’s sexual function and severity of menopausal symptoms

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150128020854N16
Enrollment
112
Registered
2025-12-03
Start date
2025-12-22
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Condition 1: Postmenopausal women’s sexual function. Condition 2: Severity of postmenopausal symptoms. Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group: Oral asparagus officinalis capsules, each capsules contains 500 mg asparagus officinalis, 3 capsules daily (One every 8 hours) for 8 weeks, constructed by Faculty o

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Being Iranian At least they should be able to read and write At least one year has passed since the last menstruation Being in the first five years of menopause Have sexual activity in the last 6 months Menopause occurs naturally (not followed by oophorectomy)

Exclusion criteria

Exclusion criteria: Taking medications such as vitamin K and potassium Using chemical or herbal drug (ginseng, vitagenus, maca, femexite capsule, flibanserin) effective on sexual function (according to the self-report) Suffering from diseases that affect sexual function such as musculoskeletal diseases, multiple sclerosis, endometriosis, diabetes, hypertension (according to the self-report) Taking hormone replacement therapy Their spouses suffer from sexual problems such as erectile dysfunction or premature ejaculation (according to the self-report) History of surgeries such as hysterectomy, oophorectomy, cystocele and rectocele, and mastectomy The presence of known psychological disorders in women and their spouses (according to the self-report) Addiction to cigarettes, alcohol or drugs Suffering from kidney diseases, chronic diarrhea and diseases that lead to malabsorption (celiac, Crohn's disease) (according to the self-report) History of fibroids or problems such as breast cancer Presence of specific events or incidents that represents a crisis in their life, such as death or incurable illness of family members, change of residence, loss of job since 6 months ago and marital infidelity, and being on the verge of divorce The occurrence of premature menopause The occurrence of speech, hearing or mental disorders that prevent communication with the researcher

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: Before the intervention, at the end of the intervention and 4 weeks later. Method of measurement: Female sexual function index.;Severity of postmenopausal symptoms. Timepoint: Before the intervention, at the end of the intervention and 4 weeks later. Method of measurement: Menopause rating scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMobina Mehrzad

Shahid Beheshti University of Medical Sciences

mobina.mehrzad@sbmu.ac.ir+98 21 8865 5366

Outcome results

None listed

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