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To Evaluate Eye Installation-Tear Free

NCT02802917 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 83

Last updated 2018-12-12

No results posted yet for this study

Summary

The primary objective of this study was to compare the human eye stinging potential of experimental formulas of sun care products \[Sun Protection Factor (SPF) 50 Y49 091, SPF 50 X15 158, SPF 50 X15 160 and SPF 50 X57 162 compared to an industry standard shampoo mixture.

Conditions

  • Sunscreening Agents

Interventions

DRUG

SPF 50 Y49 091 (BAY 987516)

5 μL of the appropriate test or control article were instilled into the lower conjunctival sac of the eye.

DRUG

SPF 50 X15 158 (BAY 987516)

5 μL of the appropriate test or control article were instilled into the lower conjunctival sac of the eye.

DRUG

SPF 50 X15 160 (BAY 987516)

5 μL of the appropriate test or control article were instilled into the lower conjunctival sac of the eye.

DRUG

SPF 50 X57 162 (BAY 987516)

5 μL of the appropriate test or control article were instilled into the lower conjunctival sac of the eye.

OTHER

J & J baby shampoo, X46 046 (control)

5 μL of the appropriate test or control article were instilled into the lower conjunctival sac of the eye.

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
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-15
Primary Completion
2015-05-24
Completion
2015-05-24

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 NCT02802917 on ClinicalTrials.gov