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

NCT02231424 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 713

Last updated 2014-09-04

No results posted yet for this study

Summary

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

Conditions

  • Pulmonary Disease, Chronic Obstructive

Interventions

DRUG

Drug: Berodual®

Sponsors & Collaborators

Eligibility

Min Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1999-01-31
Primary Completion
1999-11-30

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02231424 on ClinicalTrials.gov