MedTrace Logo

Safety Study for an All-in-One Body and Personal Lubricant

NCT01189617 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2017-02-27

Study results available
· View outcomes & findings →

Summary

This is a one-week study designed to test the safety of an all-in-one body and personal lubricant product during in-home use.

Conditions

  • Lubricating Agents

Interventions

DEVICE

Formula PD-F-7619

Off-White to Beige Lotion

Sponsors & Collaborators

  • Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc.

    lead INDUSTRY

Principal Investigators

  • Sherryl Frisch · Johnson & Johnson Consumer and Personal Products Worldwide

  • Melissa Israel · Johnson & Johnson Consumer and Personal Products Worldwide

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-06-30
Primary Completion
2010-06-30
Completion
2010-08-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT01189617 on ClinicalTrials.gov