ClinicalTrials.Veeva

Menu

A Study in Taiwan Based on Medical Records That Looks at the Occurrence of Flare-ups in Patients With Chronic Obstructive Pulmonary Disease (COPD) Who Started LABA/LAMA or LAMA Treatment

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Pulmonary Disease, Chronic Obstructive

Treatments

Drug: LAMA
Drug: Tiotropium + Olodaterol
Drug: Other LABA/LAMA

Study type

Observational

Funder types

Industry

Identifiers

NCT04011475
1237-0086

Details and patient eligibility

About

Study to collect the data on Chronic Obstructive Pulmonary Disease (COPD) patients who were administered with Long-Acting Beta-Agonist/ Long-Acting Muscarinic Antagonist (LABA/LAMA) (Fixed-dose Combination (FDC) or free combo) or LAMA treatment

Enrollment

1,617 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients who fulfil ALL the following criteria are included.

  1. Patients who diagnosed with COPD who were prescribed with LABA/LABA (FDC or free combo) as a new initiation or switching from other therapy (i.e., single/dual/triple), or newly receiving LAMA treatment for 3 months at least prior to 30 June 2018
  2. Male or female patients ≥ 40 years of age

Exclusion criteria

  1. Patients who meet the following criterion are not included.
  • Patients with documented diagnosis of bronchial asthma, asthma-COPD overlap syndrome (ACOS), bronchiectasis, cystic fibrosis, or lung cancer

Trial design

1,617 participants in 3 patient groups

Subjects with Tiotropium and Olodaterol
Treatment:
Drug: Tiotropium + Olodaterol
Subjects treated with other LABA/LAMA therapy
Treatment:
Drug: Other LABA/LAMA
Subjects treated with LAMA therapy
Treatment:
Drug: LAMA

Trial documents
1

Trial contacts and locations

12

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems