Evaluation of the effect of oral product of silk (Bombyx mori L. Cocoon), on sexual dysfunction and Quality of Life in women of reproductive age

Phase 3

Recruiting

• Conditions: sexual dysfunction.; Sexual dysfunction not due to a substance or known physiological condition

• Registration Number: IRCT20221017056213N1
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 74

Inclusion Criteria

Women aged 18-50 years
The woman being married and her husband being monogamous
FSFI women's sexual function index score<28 in the initial evaluation
Ability to read, understand and complete the questionnaire
People with BMI less than 30
Having informed consent to enter the study

Exclusion Criteria

pregnancy and breastfeeding
delaying menstruation for 2 months or more
significant clinical findings in physical examination, screening tests or other findings that prevent safe participation in the study, including the presence of any organic, anatomical disease (such as malformation of the anatomy of the external genitalia, spinal cord injuries or related surgery), hormonal in the study group such as diabetes, cerebrovascular disease, liver and kidney function damage, heart disease, hypothyroidism, cancers in history and medical history of psychiatric diseases that are under drug treatment.
receiving psychotherapy or other treatments for sexual dysfunction
using tobacco, alcohol, drug abuse
using any chemical and herbal medicine known to affect libido
being participate in another clinical trial study
major changes in recent relationships, ongoing or unforeseeable disorder or disturbance that is not related to his sexual dysfunction.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sexual dysfunction. Timepoint: The beginning of the study, the end of the fourth week from the beginning of the intervention, one month after the end of the intervention. Method of measurement: female sexual function index Questionnaire.;Quality of Life. Timepoint: The beginning and end of the study. Method of measurement: Quality of life questionnaire with 36 questions.