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

Completed · Not applicable

Conditions studied: Coitus

In brief

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

Key facts

Study ID

NCT00778934

Run by

Johnson & Johnson Consumer and Personal Products Worldwide

People needed

79

Starts

2007-12-01

Expected to finish

2008-04-01

Last updated by the study team

2011-10-06

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

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

You may not qualify if…

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

Where it is running

• Center of Marital and Sexual Health of South Florida — West Palm Beach, Florida, United States
• Center for Marital and Sexual Health, Inc. — Beachwood, Ohio, United States

Full record on ClinicalTrials.gov

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