Postmarketing Surveillance Study of Berodual® Metered-dose Inhaler in Chronic Obstructive Respiratory Tract Disease

NCT ID: NCT02232594

Last Updated: 2014-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

834 participants

Study Classification

OBSERVATIONAL

Study Start Date

2000-01-31

Brief Summary

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The aim of this postmarketing surveillance is to obtain further information about the tolerability and efficacy of Berodual® metered-dose inhaler in the treatment of chronic obstructive respiratory tract disease under conditions of daily practice

Detailed Description

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Conditions

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Pulmonary Disease, Chronic Obstructive

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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chronic obstructive respiratory tract disease patients

Berodual®

Intervention Type DRUG

Interventions

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Berodual®

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients of either sex over 40 years with the symptoms of a chronic obstructive airways disease
* Only patients which have not been treated with Berodual® within the last year should be included

Exclusion Criteria

* Contraindications listed in the Instructions for Use/Summary of Product Characteristics for Berodual® metered-dose inhaler
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Boehringer Ingelheim

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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215.1358

Identifier Type: -

Identifier Source: org_study_id

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