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

NCT00778934 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 79

Last updated 2011-10-06

No results posted yet for this study

Summary

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

Conditions

  • Coitus

Interventions

OTHER

Intimate Health Gel

Intimate Health Gel

Sponsors & Collaborators

  • Johnson & Johnson Consumer and Personal Products Worldwide

    lead INDUSTRY

Principal Investigators

  • Rita Wanser · J&J CPPW

Study Design

Allocation
NA
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2008-02-29
Completion
2008-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00778934 on ClinicalTrials.gov