Specific Use-result Surveillance of Spiriva Respimat in Asthmatics

NCT02489981 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 359

Last updated 2019-02-11

Study results available
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Summary

The safety of Spiriva® 2.5 µg Respimat® 60 puffs (hereinafter referred to as Spiriva® Respimat®) in patients with severe persistent asthma under the real-world use was not confirmed in clinical trials.

Conditions

Interventions

DRUG

Spiriva

60 puffs

Sponsors & Collaborators

Principal Investigators

  • Boehringer Ingelheim · Boehringer Ingelheim

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-01
Primary Completion
2017-08-01
Completion
2017-09-28

Countries

  • Brazil

Study Locations

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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 NCT02489981 on ClinicalTrials.gov