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Postmarketing Surveillance Study of Atrovent® Inhalets in Chronic Obstructive Pulmonary Disease

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Pulmonary Disease, Chronic Obstructive

Treatments

Drug: Atrovent® inhalets

Study type

Observational

Funder types

Industry

Identifiers

NCT02238171
244.2497

Details and patient eligibility

About

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

346 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 had not been treated with Atrovent® within the last year were to be considered for inclusion

Exclusion criteria

• Contraindications listed in the Instructions for Use/Summary of Product Characteristics for Atrovent® Inhalets

Trial design

346 participants in 1 patient group

Chronic Obstructive Pulmonary Disease
Treatment:
Drug: Atrovent® inhalets

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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