Topical Agent for Treatment of Red Skin

NCT ID: NCT00279890

Last Updated: 2011-05-23

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

PHASE1

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-07-31

Study Completion Date

2007-01-31

Brief Summary

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SR-01 may reduce facial redness. it is a topically applied product. The agent will be applied to local skin areas of subjects with red facial skin to assess affect, and then applied to the whole face to assess efficacy and safety

Detailed Description

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Conditions

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Rosacea Bilaterally Symmetric Red Skin on Cheeks

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Topical SR-01

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Bilaterally symmetric red skin on cheeks Caucasian Age 18-60 years
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Mayo Clinic

Principal Investigators

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Mark V. Dahl, M.D.

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

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Mayo Clinic

Scottsdale, Arizona, United States

Site Status

Countries

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United States

Other Identifiers

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MCS 385

Identifier Type: -

Identifier Source: secondary_id

44-05

Identifier Type: -

Identifier Source: org_study_id

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