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Supervised Outdoor-Use Test For Sunscreen Products in Adults

NCT02877511 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 102

Last updated 2018-12-13

No results posted yet for this study

Summary

To assess the safety of a sunscreen product under supervised outdoor-use conditions

Conditions

  • Sunscreening Agents

Interventions

DRUG

BAY987517

Applied liberally to the skin (Formulation: Y73-161

DRUG

Sunscreen Lotion (Y65-110)

Applied liberally to the skin

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-20
Primary Completion
2016-08-21
Completion
2016-08-21

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT02877511 on ClinicalTrials.gov