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Clinical Trials/NCT00643630
NCT00643630
Completed
Not Applicable

A Study to Determine the Skin Barrier Effect of Tetrix Cream

Coria Laboratories, Ltd.1 site in 1 country36 target enrollmentStarted: October 2007Last updated:
ConditionsHealthy

Overview

Phase
Not Applicable
Status
Completed
Enrollment
36
Locations
1
Primary Endpoint
Prevention of delayed bype hypersensitivity reaction following application of antigen

Overview

Brief Summary

To determine if Tetrix Cream,, when applied to the skin, acts as a barrier to prevent injury to the skin

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Normal subjects who are sensitized to nickel, neomycin, or fragrance mix.

Exclusion Criteria

  • Under 18 years of age.

Outcomes

Primary Outcomes

Prevention of delayed bype hypersensitivity reaction following application of antigen

Time Frame: up to 96 hours after antigen application

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry

Study Sites (1)

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