CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 43 enrolled
Drug / intervention
Beclomethasone Dipropionate/Formoterol Fumaratedrug
Likely dose
Beclomethasone Dipropionate/Formoterol Fumarate 6 μgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04421742
NCT04421742N/ACompleted

The Effect of Beclomethasone/Formoterol in Extra-fine Formulation on Quality of Life and Dyspnea is Associated to the Improvement in Small Airway Dysfunction in COPD Patients. A Pilot Study (IOSCOPD20161102)

Alfredo Antonio Chetta·observational·Posted Jun 9, 2020·Updated Jun 9, 2020

In Brief

An observational study evaluating Beclomethasone Dipropionate/Formoterol Fumarate for Chronic Obstructive Pulmonary Disease. Completed, enrolled 43 participants across 1 site.

Detailed Summary

In patients with chronic obstructive pulmonary disease (COPD), small-airway dysfunction (SAD) is considered a key element and a functional consequence of the pathology. However, the exact role of SAD as a specific 'pharmacological target' is not yet fully known. Objectives In an open-label prospective study, we aimed to ascertain whether an extra-fine formulation of Beclomethasone dipropionate/Formoterol fumarate (BDP/FF) NEXThaler® 100/6 μg b.i.d. can improve the impact of the disease on the quality of daily life of COPD patients, acting on SAD. Methods We studied COPD patients with severe airflow obstruction and 1 moderate exacerbation in the previous year, being treated with BDP/FF NEXThaler® for 12 weeks. They underwent three visits, at the start of the treatment (V1), at 6th week (V2) and at 12th week (V3). By the impulse oscillometry system and by spirometry and plethysmography we measured at each visit the fall in resistance from 5 to 20 Hz (R5-R20) and the residual volume/total lung capacity (RV/TLC). COPD Assessment Test (CAT) and the modified Medical Research Council (mMRC) questionnaire were also measured at each visit to assess the impact of the disease on the quality of life of the patients.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesItaly
CollaboratorsUniversity of Parma

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJun 9, 2020
Enrollment StartMay 31, 2017
Primary CompletionFeb 8, 2019
Study CompletionMay 23, 2019
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 6.1 years ago

Interventions

Beclomethasone Dipropionate/Formoterol Fumaratedrug

BDP/FF NEXThaler® 100/6 μg b.i.d.