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NT-proBNP Levels During Triple Therapy With Formoterol/Glycopyrrolate/Budesonide in Patients With COPD. — NTproBNP  

COPD Clinical Trial

Official title:
Change in Serum Levels of NT-proBNP During Triple Therapy With Formoterol/Glycopyrrolate/Budesonide in Patients With COPD.

Clinical Trial Summary

Observational prospective study to evaluate serum NT-proBNP levels in a population of COPD patients three months after the iniation of triple inhaled formoterol/glycopyrrolate/budesonide therapy.

Clinical Trial Description

The purpose of the trixeo study is to conduct a prospective observational study to evaluate serum NT-proBNP levels in a population of COPD patients three months after the initiation of triple inhaled formoterol/glycopyrrolate/budesonide therapy. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06317428
Study type Observational
Source Istituto Nazionale di Ricovero e Cura per Anziani
Contact Anna Rita Bonfigli
Phone 0718003719
Email a.bonfigli@inrca.it
Status Recruiting
Phase
Start date June 28, 2022
Completion date December 31, 2025
View Details
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