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Evaluation of the Irritation Potential of Products in Human Eyes

NCT02714166 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2017-03-30

No results posted yet for this study

Summary

To evaluate the human eye irritation potential of one test sunscreen formulation.

Conditions

  • Sunscreening Agents

Interventions

OTHER

Sunscreen lotion SPF (Sun Protection Factor) 50 (BAY987521)

Study staff will administer the control in one eye and a test sunscreen in the other eye according to the assigned randomization schedule.

OTHER

Ophthalmic Ointment

Study staff will administer the control in one eye and a test sunscreen in the other eye according to the assigned randomization schedule.

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-02-26
Primary Completion
2016-02-26
Completion
2016-02-26

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 NCT02714166 on ClinicalTrials.gov