In-Home Use Study to Evaluate Use of an Intimate Health Product in Females

Johnson & Johnson (J&J)

Status: Completed

Conditions: Coitus

Treatments: Other: Intimate Health Gel

Study type: Interventional

Funder types: Industry

Identifiers

NCT00778934

CA-P-5739-1

Details and patient eligibility

About

The purpose of this study is to evaluate the effects of an intimate health product on sexual experience in females.

Full description

Study to evaluate consumer perceptions of a cosmetic intimate health product on sexual experience in females, using a validated psychometric questionnaire.

Enrollment: 79 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Normal, healthy females >18 years of age
• In committed heterosexual relationship for >6months
• Of adequate sexual functioning
• On acceptable method of birth control

Exclusion criteria

• Pregnant or breastfeeding
• Allergy to product ingredients
• Irritation or infection in genital area
• Unstable or uncontrolled medical condition

Trial design

79 participants in 1 patient group

1

Experimental group

Description:

Intimate Health Gel

Treatment:

Other: Intimate Health Gel