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NCT02292797 Clinical Trial

Assessment of the Rosacea Prevalence in the General Population

Rosacea Clinical Trial

— RISE  

Official title:
Assessment of the Prevalence of Rosacea in the General Population

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02292797
Other study ID # RD.03.SPR.29104
Secondary ID
Status Completed
Phase N/A
First received October 14, 2014
Last updated November 14, 2014
Start date September 2013
Est. completion date February 2014

Study information
Verified date November 2014
Source Galderma
Contact n/a
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés
Study type Observational

Clinical Trial Summary

Multi-centre interventional cross-sectional prevalence study Assessment of the Rosacea Prevalence in the General Population.

Description:

Primary objective:

Assessment of the prevalence of rosacea in the general population per country using subject questionnaire and dermatologist diagnosis

Recruitment information / eligibility
Status Completed
Enrollment 6000
Est. completion date February 2014
Est. primary completion date February 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Part I

Inclusion Criteria:

The following subjects will be included in the study:

- Subjects aged 18 to 65 years old from the general population

- Subjects who are willing to complete the questionnaires

Part II

Inclusion Criteria:

The following subjects will be included in Part II of the study:

- Subjects who screened positive for rosacea during the first part of the study and selected by random method

- Subjects who gave their informed consent to participate in Part II of the study

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Other:
• Prevalence assessment
Assessment of the prevalence of rosacea in the general population per country using subject questionnaire and dermatologist diagnosis

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Galderma

Outcome
Type Measure Description Time frame Safety issue
Primary percentage of subjects with rosacea diagnosis confirmed estimation of the percentage of rosacea patients in the general population general population will be surveyed over an expected average duration of 6 months No
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