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Evaluation the Effect of Fenugreek Vaginal Cream on Vaginal Atrophy in Postmenopausal Women

Evaluation the Effect of Fenugreek Vaginal Cream on Vaginal Atrophy in Postmenopausal Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017010331705N2
Enrollment
60
Registered
2017-02-09
Start date
2017-01-20
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

Atrophy Vaginal in post menopausal women. Postmenopausal Atrophic Vaginitis

Interventions

Intervention 1: Cream Vaginal Fenugrrek 5% one Applicator daily for 8 week. Intervention 2: control group (placebo) one applicator daily for 8week.
Treatment - Drugs
Placebo
Cream Vaginal Fenugrrek 5% one Applicator daily for 8 week
control group (placebo) one applicator daily for 8week

Sponsors

Vice chancellor for research, Ahwaz JundiShapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: inclusion criteria: Age between 45 to 65; Amenorrhea at less 12 month or have hormone test with FSH level more than 40 unit; Presenting symptom of vaginal atrophy; Have Sexual activity and single partner; Exclusion criteria; Vaginal infection? Genital Abnormalities? The use of Sex Hormones within the 8 weeks preceding studY; user of smoke and alcohol and etc; Genital Bleeding or spotting of unknown Cause; Use of Phytoestrogens such as Soy; Red clove; Fenugreek; Vitex within the last one Month.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Percentage of Maturity vaginal. Timepoint: Before and after eight weeks (end of intervention). Method of measurement: Vaginal smear.;Vaginal Atrophy. Timepoint: Before intervention, Two weeks after the intervention, Four weeks after intervention, Eight weeks after intervention. Method of measurement: Kupperman Index Questionnaire.;Vaginal PH. Timepoint: Before and after eight weeks (end of intervention). Method of measurement: By PH meter strips.

Secondary

MeasureTime frame
Sexual function. Timepoint: Before and after intervention. Method of measurement: Female Sexual Function Index (FSFI) questionnaire.;Temperament. Timepoint: Before and after intervention. Method of measurement: Temperament questionnaires.;Dyspareunia. Timepoint: Before intervention, Two weeks after the intervention, Four weeks after intervention, Eight weeks after intervention. Method of measurement: self-assessed 4-point scale of composite score.;Menopausal symptoms. Timepoint: Before intervention, 2, 4, 8 weeks after intervention. Method of measurement: Kupperman Index Questionnaire.;Severity of menopausal symptoms. Timepoint: Before intervention, 2, 4, 8 weeks after intervention. Method of measurement: Menopause Rating Scale (MRS) questionnaire.;Sexual satisfaction. Timepoint: Before and after intervention. Method of measurement: Larson's sexual satisfaction questioner.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFakhriyeh Mazalzadeh

Ahvaz Jundishapur University of Medical Sciences

mazal.f@ajums.ac.ir+98 61 3443 9419

Outcome results

None listed

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