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Mirvaso® Utilisation and Patient Satisfaction Evaluation (MUSE) (MUSE)

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ClinicalTrials.gov Identifier: NCT02637232
Recruitment Status : Completed
First Posted : December 22, 2015
Last Update Posted : May 18, 2016
Sponsor:
Collaborator:
Chiltern International Inc.
Information provided by (Responsible Party):
Galderma

Brief Summary:
The aim of the study is to evaluate the level of satisfaction among patients to whom Mirvaso® / Onreltea TM (trade mark) is prescribed.

Condition or disease Intervention/treatment
Rosacea Other: Mirvaso® / Onreltea TM

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Study Type : Observational
Actual Enrollment : 302 participants
Time Perspective: Prospective
Official Title: Mirvaso® Utilisation and Patient Satisfaction Evaluation
Study Start Date : October 2015
Actual Primary Completion Date : May 2016
Actual Study Completion Date : May 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Rosacea

Group/Cohort Intervention/treatment
Mirvaso® / Onreltea TM Other: Mirvaso® / Onreltea TM



Primary Outcome Measures :
  1. Satisfaction among patients to whom Mirvaso®/OnrelteaTM is prescribed (% of subjects across score per question). [ Time Frame: Week 4 ]
    % of subjects across score per question.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patient with persistent facial erythema of rosacea
Criteria

Inclusion Criteria:

  • Patients to whom the physician has already decided to prescribe Mirvaso® /OnrelteaTM according to package insert

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02637232


Locations
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Canada
Investigator site 1
Hamilton, Canada
Sponsors and Collaborators
Galderma
Chiltern International Inc.

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Responsible Party: Galderma
ClinicalTrials.gov Identifier: NCT02637232     History of Changes
Other Study ID Numbers: RD.03.SPR.104160
First Posted: December 22, 2015    Key Record Dates
Last Update Posted: May 18, 2016
Last Verified: May 2016

Additional relevant MeSH terms:
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Rosacea
Skin Diseases
Brimonidine Tartrate
Antihypertensive Agents
Adrenergic alpha-2 Receptor Agonists
Adrenergic alpha-Agonists
Adrenergic Agonists
Adrenergic Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs