REported Outcomes in COPD with Trixeo in Real worlD in Germany - RECORD

Study identifier:D5980R00037

ClinicalTrials.gov identifier:NCT05311306

EudraCT identifier:N/A

CTIS identifier:N/A

Recruitment Complete

Official Title

A non-interventional, multi-centre study to investigate the change in clinical and patient-reported outcomes in moderate to severe COPD patients treated with TRIXEO (Budesonide / Glycopyrronium / Formoterol) under real-life conditions

Medical condition

Chronic Obstructive Pulmonary Disease

Phase

N/A

Healthy volunteers

No

Study drug

-

Sex

All

Actual Enrollment

466

Study type

Observational

Age

18 Years - n/a

Date

Study Start Date: 15 Mar 2022
Estimated Primary Completion Date: 30 Jun 2024
Estimated Study Completion Date: 30 Jun 2024

Study design

Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Feb 2024 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria