Investigating the effect of the hydro alcoholic extract of the flower of Elaeagnus angustifolia L on the sexual performance of wome

Phase 3

Conditions: Decreased sexual performance in women.
Hypoactive sexual desire disorder
F52.0

Registration Number: IRCT20230501058039N1

Lead Sponsor: Kermanshah University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: Female

Target Recruitment: 58

Inclusion Criteria

Married
Having a constant sexual partner
Healthy pelvic examination
Age 18 to 54
Deficiency or loss of sexual desire caused by stress
Normal and regular menstrual cycle
Obtaining a score less than 28 from the sexual dysfunction questionnaire.

Exclusion Criteria

Pregnancy and breastfeeding
Menopause
Oophorectomy
Consumption of alcohol and tobacco
Wife's sexual problem
Getting any disease during the study
The patient's unwillingness to continue
Diabetes, kidney and liver diseases, hypothyroidism, cardiovascular-cerebrovascular disease, cancer, mental disorder with drug use, use of any contraceptive and hormone-based drugs that affect libido, such as androgens, anti-androgens, SSRI , tricyclic antidepressants, progestin's and a-blockers a

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of changes in the total score and domains of the sexual function questionnaire (FSFI) after consuming the hydro alcoholic extract of Elaeagnus angustifolia L. Timepoint: The total score of the questionnaire will be checked before taking the medicine and 30 days after taking the medicine. Method of measurement: Rosen sexual function questionnaire.

Secondary Outcome Measures

Name	Time	Method
Comparison of progesterone and estrogen hormone changes. Timepoint: The amount of hormones will be measured once at the beginning of the study and once after 30 days at the end of the study. Method of measurement: Monobind kit.