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Nasonex? Nasal Suspension 50 ?g Long-term Designated Drug Use Investigation

This study is currently Recruiting

October 2011 By Schering-Plough

First Recieved on May 14, 2009

Last Updated on October 31, 2011

Sponsor: Schering-Plough
Collaborators:
Information provided by: Schering-Plough
Identifier: NCT00903721

Purpose

The investigation will be conducted to define safety and efficacy under the conditions of post-marketing use of this drug in subjects with allergic rhinitis. Post-marketing surveys are not considered applicable clinical trials and thus the results of this survey will not be posted at its conclusion. The results will be submitted to public health officials as required by applicable national and international laws.

Study Type: Observational
Study Design: Observational Model: Cohort, Time Perspective: Prospective

Eligibility

Ages Eligible for Study:N/A
Genders Eligible for Study:Both
Accepts Healthy Volunteers:No
Criteria

Inclusion Criteria: - Patients who are treated with Nasonex for perennial or seasonal allergic rhinitis. Exclusion Criteria: - Patients with an infection for which there is no effective antimicrobial drug or systemic fungal infection [symptoms may exacerbate] - Patients with a history of hypersensitivity to any ingredient of this drug

Investigators

Locations

  • Coordinating Location

    Osaka, Japan

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