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The effect of Rosa damascena mill on menopausal symptoms

The effect of oral capsules Rosa damascena mill extract on menopausal symptoms

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210208050295N1
Enrollment
78
Registered
2021-03-03
Start date
2021-04-21
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

menopausal symptoms. Any condition of the genital system affecting females, caused by pathological changes associated with the perimenopausal period, such as the permanent cessation of menstruation and infertility. Includes: Symptoms such as flushing, sleeplessness, headache,

Interventions

Intervention 1: Intervention group: In this group, research units take a 500 mg capsule containing Rosa damascena mill hydro-alcoholic extract every 12 hours for 8 weeks. These capsules are prepared i

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Having a minimum education in primary school Age 45 to 65 years old Having a normal menopause (stopping menstruation for at least one year after 45 years old, without interfering with pregnancy and lactation, surgery, medication and pathology) Married and living with her husband Having sexual intercourse in the last month Obtained at least 5 score from the initial MRS Lack of known and treated medical diseases which affect the results of the study (cardiovascular, liver, kidney, chronic lung disorders, thyroid, neurology and psychiatry diseases, musculoskeletal, pelvic prolapse, urinary disorders and neurological diseases known and treated ) No history of cancer

Exclusion criteria

Exclusion criteria: Drug addiction, smoking and alcohol abuse Taken medicine that improve menopausal symptoms in the last 6 months (Such as estrogen and progesterone, GnRH agonists and antagonists, clonidine, gabapentin, serotonin and norepinephrine inhibitors, paroxetine, venlafaxine, vitamin E, methyldopa, naloxone and tibolone) Use of complementary medicine to improve menopausal symptoms (such as herbs, acupuncture and acupressure) during the last 6 months Women professional athletes or women with severe mobility limitations who are unable to do housework

Design outcomes

Primary

MeasureTime frame
Severity of menopause symptoms. Timepoint: At the beginning of the study (before the start of the study) and at the beginning of weeks 4 and 8 after the start of the study. Method of measurement: Menopause raring scale.

Secondary

MeasureTime frame
Depression, anxiety and stress in menopausal women. Timepoint: At the beginning of the study (before the start of the study) and at the beginning of weeks 4 and 8 after the start of the study. Method of measurement: Depression, Anxiety and Stress Scale.;Quality of sleep in menopausal women. Timepoint: At the beginning of the study (before the start of the study) and at the beginning of weeks 4 and 8 after the start of the study. Method of measurement: Pittsburgh Sleep Quality Index.;Sexual function in menopausal women. Timepoint: At the beginning of the study (before the start of the study) and at the beginning of weeks 4 and 8 after the start of the study. Method of measurement: Female sexual function index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Gholinezhad

Mashhad University of Medical Sciences

Gholinezhadz982@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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