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NT-proBNP Levels During Triple Therapy With Formoterol/Glycopyrrolate/Budesonide in Patients With COPD. - Trial NCT06317428

Access comprehensive clinical trial information for NCT06317428 through Pure Global AI's free database. This phase not specified trial is sponsored by Istituto Nazionale di Ricovero e Cura per Anziani and is currently Recruiting. The study focuses on COPD. Target enrollment is 29 participants.

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NCT06317428
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Trial Details
ClinicalTrials.gov โ€ข NCT06317428
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NT-proBNP Levels During Triple Therapy With Formoterol/Glycopyrrolate/Budesonide in Patients With COPD.
Change in Serum Levels of NT-proBNP During Triple Therapy With Formoterol/Glycopyrrolate/Budesonide in Patients With COPD.

Study Focus

COPD

Observational

Sponsor & Location

Istituto Nazionale di Ricovero e Cura per Anziani

Ancona,Osimo, Italy

Timeline & Enrollment

N/A

Jun 28, 2022

Dec 31, 2025

29 participants

Primary Outcome

Change in serum NT-pro-BNP levels

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.

ICD-10 Classifications

Chronic obstructive pulmonary disease, unspecified
Other chronic obstructive pulmonary disease
Other specified chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease with acute exacerbation, unspecified
Pulmonary heart disease, unspecified

Data Source

ClinicalTrials.gov

NCT06317428

Non-Device Trial