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A Study of Patient Concerns and Treatment Satisfaction in Patients Being Treated With Finacea Foam for Rosacea

A Study of Patient Concerns and Treatment Satisfaction in Patients Being Treated With Finacea Foam for Rosacea

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03193372
Enrollment
2200
Registered
2017-06-20
Start date
2017-07-20
Completion date
2017-11-15
Last updated
2020-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rosacea

Brief summary

To survey rosacea patients about their concerns, treatment satisfaction, and quality of life associated with their Finacea Foam treatment

Interventions

DRUGAzelaic Acid (Finacea Foam, BAY39-6251)

Finacea Foam, Active substance Azelaic acid

Sponsors

Bayer
CollaboratorINDUSTRY
LEO Pharma
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* At least 18 years of age * Diagnosis of rosacea by a medical professional * Currently using Finacea Foam as topical monotherapy for rosacea * Willing and able to provide voluntary, informed consent to participate in this study

Exclusion criteria

\- Use of any other topical treatment for rosacea at the time of enrollment

Design outcomes

Primary

MeasureTime frameDescription
Demographics and clinical characteristicsone-time survey in 2 week recruitment windowCollected patient demographics and characteristics are : * Year of birth * Gender * Insurance type
Rosacea-relevant comorbidities and complicationsone-time survey in 2 week recruitment windowPatient reported history of the following will be collected : * Blepharitis * Conjunctivitis * Corneal neovascularization/keratitis * Depression * Migraine
Rosacea subtypeone-time survey in 2 week recruitment windowPatient reported diagnosis of the following will be collected: * Erythematotelangiectatic (facial redness) * Papulopustular (bumps and pimples) * Phymatous (enlargement of the nose) * Ocular (eye irritation) * Unknown
Past use of topical rosacea treatmentsone-time survey in 2 week recruitment windowPatient reported use of the following medications will be collected: * Metronidazole gel * Metronidazole cream * Metronidazole lotion * Metronidazole emulsion * Brimonidine tartrate gel
Patient concerns collected by Rosacea Treatment Preference Questionnaireone-time survey in 2 week recruitment windowRosacea Treatment Preference Questionnaire is a survey to assess patient self-reported rosacea subtype and severity, and to evaluate the concerns that contribute to patient satisfaction/dissatisfaction, as well as treatment decisions with rosacea topical treatments
Treatment satisfaction assessed by Satisfaction with Medicines Questionnaire (SATMED-Q)one-time survey in 2 week recruitment windowSATMED-Q is a 17-question, validated, multidimensional generic questionnaire designed for use in patients with any chronic disease treated with medicines
Quality of life measured by Dermatology Life Quality Index (DLQI)one-time survey in 2 week recruitment windowDLQI is a widely used dermatology-related quality of life tool

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026