Menopause. Menopausal and other perimenopausal disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women who have had at least one year since their last menstrual period. Having an active sexual partner and consenting to participate in the study. Not having severe chronic diseases (uncontrolled diabetes, advanced heart disease, severe neurological and mental disorders). Not having a history of allergy to lactofem. Not taking hormonal medications that affect sexual function.
Exclusion criteria
Exclusion criteria: Allergies or side effects from Lactofem. Significant changes in health status that could affect the results. Unwillingness to continue participating in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Female sexual function score based on the Female Sexual Function Index (FSFI) before and after the intervention. Timepoint: Female sexual function will be assessed before the intervention and six weeks after the end of the intervention. Method of measurement: Female sexual function will be assessed using the Female Sexual Function Index (FSFI) .;Women's sexual satisfaction score is assessed using the standard Hudson questionnaire before and after the intervention. Timepoint: Female sexual satisfaction will be assessed before the intervention and six weeks after the end of the intervention. Method of measurement: Female sexual satisfaction will be assessed using the Hudson Sexual Satisfaction Questionnaire . | — |
Countries
Iran (Islamic Republic of)
Contacts
Yasouj University of Medical Sciences