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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06060691
Other study ID # 5/23
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date September 20, 2023
Est. completion date February 1, 2024

Study information

Verified date May 2024
Source Deraya University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the quality of sexual life of females with sexual interest or arousal disorder before and after accurate application of a formulated emulgel made from natural ingredients, including kaempferol as an API


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 1, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 28 Years to 45 Years
Eligibility Inclusion Criteria: - Women between the ages of 28 and 45 - had regular periods and previous menstrual bleeding lasted between three and seven days Exclusion Criteria: - sensitivity to drug of therapy, - cancer, - autoimmune illness, - smoking or drinking, - liver disease, - irregular menstruation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Kaempferol
Kaempferol

Locations

Country Name City State
Egypt Soad A. Mohamad Minya

Sponsors (1)

Lead Sponsor Collaborator
Deraya University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Female Sexual Function Index The FSFI comprises 19 questions of sexual function in six independent areas consisting of desire, arousal, lubrication, orgasm, sexual satisfaction , pain from sex. two months
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