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Evaluation of the Stinging Potential of Products in Human Eyes

NCT02872194 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2018-12-12

No results posted yet for this study

Summary

The objective of this study was to compare the human eye stinging potential of experimental formulas and an industry standard shampoo mixture. The study was conducted under the supervision of a Board Certified Ophthalmologist. The study design was a three cell, single blind study. Subjects were given the industry standard shampoo mixture in one eye and an exploratory sunscreen in the other as according to the randomization schedule.

Conditions

  • Sunscreen Agents

Interventions

DRUG

BAY987516, Y55-170

10 uL in one eye

DRUG

BAY987516, X72-151

10 uL in one eye

DRUG

BAY987516, Y49-034

10 uL in one eye

DRUG

Standard shampoo mixture (control)

10 uL in one eye

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2014-09-05
Primary Completion
2014-09-06
Completion
2014-09-06

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 NCT02872194 on ClinicalTrials.gov