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Post-marketing Surveillance of Atrovent® in Chronic Obstructive Pulmonary Disease

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Boehringer Ingelheim

Status

Completed

Conditions

Pulmonary Disease, Chronic Obstructive

Treatments

Drug: Atrovent® - inhalets

Study type

Observational

Funder types

Industry

Identifiers

NCT02233881
244.2501

Details and patient eligibility

About

Study to obtain further information on the tolerability and efficacy of Atrovent® inhalets in the treatment of Chronic Obstructive Pulmonary Disease under conditions of daily practice

Enrollment

4,222 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients of both gender older than 40 years, who suffer from Chronic Obstructive Pulmonary Disease
  • Only patients who have not been treated with Atrovent® within the last year are to be considered for inclusion

Exclusion criteria

  • Contraindications listed in the Instructions for Use/Summary of Product Characteristics for Atrovent® metered dose inhaler

Trial design

4,222 participants in 1 patient group

Chronic obstructive pulmonary disease patients
Treatment:
Drug: Atrovent® - inhalets

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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