the Ameliorating Effects of Antioxidant Gel on Female Arousal Disorder and Sexual Dysfunction

Deraya University

Status and phase: Completed; Phase 1

Conditions: Female Sexual Dysfunction

Treatments: Drug: Kaempferol

Study type: Interventional

Funder types: Other

Identifiers

NCT06060691

5/23

Details and patient eligibility

About

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

Enrollment: 30 patients

Sex: Female

Ages: 28 to 45 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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30 participants in 2 patient groups, including a placebo group

Kaempferol group

Experimental group

Description:

Kaempferol gel received the vaginal gel containing antioxidant extract every day for seven days. Then, the treatment continued for two months, twice weekly

Treatment:

Drug: Kaempferol

Placebo group

Placebo Comparator group

Description:

Plain formulation received the vaginal gel containing antioxidant extract every day for seven days. Then, the treatment continued for two months, twice weekly

Treatment:

Drug: Kaempferol