Mirvaso® Utilisation and Patient Satisfaction Evaluation (MUSE)

NCT ID: NCT02637232

Last Updated: 2021-05-28

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

301 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-10-31

Study Completion Date

2016-05-31

Brief Summary

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

Detailed Description

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Conditions

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Rosacea

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Mirvaso® / Onreltea TM

Mirvaso® / Onreltea TM

Intervention Type OTHER

Interventions

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Mirvaso® / Onreltea TM

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients to whom the physician has already decided to prescribe Mirvaso® /OnrelteaTM according to package insert
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chiltern International Inc.

INDUSTRY

Sponsor Role collaborator

Galderma R&D

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Investigator site 1

Hamilton, , Canada

Site Status

Countries

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Canada

Other Identifiers

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RD.03.SPR.104160

Identifier Type: -

Identifier Source: org_study_id

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