Repeat Insult Patch Test for Daily Advance Cetaphil Moisturizing Lotion

NCT ID: NCT01892423

Last Updated: 2022-07-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

146 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-08-31

Brief Summary

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Human repeat insult patch test to assess the potential for Cetaphil Moisturizing Lotion Daily Advance to induce sensitization to the skin

Detailed Description

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Conditions

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Skin Irritation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Cetaphil Moisturizing Lotion Daily Advance

Each subject had Cetaphil Moisturizing Lotion Daily Advance applied

Group Type EXPERIMENTAL

Cetaphil Moisturizing Lotion Daily Advance

Intervention Type OTHER

Interventions

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Cetaphil Moisturizing Lotion Daily Advance

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age 18-65 years
* Good health
* willingness to cooperate and participate
* willingness to avoid topical products at test sites
* willingness to avoid direct sun exposure to test sites

Exclusion Criteria

* Individuals with active psoriasis or eczema
* individuals with sunburn, acne, abrasions, scar tissue, or tattoos on test sites, or disease of skin that might interfere
* individuals who have had a mastectomy with axillary nodes were removed
* individuals receiving anticancer, immunosuppressive treatments or medications, or radiation
* pregnant, nursing, or planned to become pregnant
* use of topical steroids or drugs at test sites
* active or untreated skin cancer
* active hepatitis
* current routine or frequent use of high doses of anti-inflammatory drugs
* individuals who have had les than two week rest period since completion of previous patch testing on upper back or upper arms
* individuals with uncontrolled metabolic diseases
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Galderma R&D

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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James H Herndon, MD, FAAD

Role: PRINCIPAL_INVESTIGATOR

Locations

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Thomas J Stephens and Associates Inc

Carrollton, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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GLI.04SPR.US10044

Identifier Type: -

Identifier Source: org_study_id

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