Condition 1: Loosening of the pelvic floor muscles. Condition 2: Sexual Dysfunction. Sexual dysfunction not due to a substance or known physiological condition
Conditions
Interventions
Intervention 1: Intervention group: Vaginal gel with a concentration of 2.5% made in the laboratory of Ahvaz School of Pharmacy is given to postmenopausal women daily for 12 weeks. Intervention 2: Con
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
45 Years to 65 Years
Inclusion criteria
Inclusion criteria: Not menstruating for the past 12 months Sexual Function score less than 26.5 Have literacy Score 28 or less with the prinometer
Exclusion criteria
Exclusion criteria: Chronic diseases Smoking and alcohol consumption Vaginal or cervical infection Getting uterine bleeding or spotting for an unknown reason Taking any type of vaginal medication Breast disease with a specific cause People with grade 3 and 4 pelvic floor muscle relaxation syndrome based on pop-Q Experiencing adverse or stressful events in a woman or her husband
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pelvic floor muscle`s strength. Timepoint: Before the intervention, 4,8and 12 weeks after the start of use of the vaginal gel of the oak Gall. Method of measurement: prinometry.;Percentage of people with improved Sexual function. Timepoint: Before the intervention, 4,8and 12 weeks after the start of use of the vaginal gel of the oak Gall. Method of measurement: Sexual Function Index Questionnaire.;Sexual Function Score in the Sexual Function index Questionnaire. Timepoint: Before the intervention, 4,8and 12 weeks after the start of use of the vaginal gel of the oak Gall. Method of measurement: Questionnaire FSFI. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSahar Omidianpour
Ahvaz University of Medical Sciences
Outcome results
None listed