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Study identifier: NCT07665931 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Simeox® on Residual Volume in COPD Patients With Pulmonary Hyperinflation

Condition: Chronic Obstructive Pulmonary Disease (COPD) · Pulmonary Hyperinflation  ·  Sponsor: Azienda Socio Sanitaria Territoriale di Lodi

PhaseNA
Planned participants23
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Brief Summary People with severe chronic obstructive pulmonary disease (COPD) often have too much air trapped in their lungs (pulmonary hyperinflation). This makes it hard to breathe and reduces quality of life. This study tests whether a single session with a medical device called Simeox® can reduce the amount of air trapped in the lungs. Simeox® works by applying gentle intermittent negative pressure during exhalation to help air move out of the lungs more easily. Patients with severe or very severe COPD and documented hyperinflation will undergo lung function measurements before and immediately after a 20-minute Simeox® session. The main measurement is the change in residual volume (RV), which is the amount of air left in the lungs after a full exhalation. We will also measure changes in other lung volumes, breathlessness, and any side effects. This is a single-arm pilot study enrolling 23 patients at one center in Italy (ASST Lodi). The study is non-profit and has been approved by the Ethics Committee Comitato Etico Territoriale Lombardia 1 (CET Lombardia 1).

This description comes directly from the study's public registry record.

Talk to the study team

Andrea Di Matteo, dr  ·  +393387123135  ·  andrea.dimatteo@asst-lodi.it

Always discuss trial participation with your own doctor first.

Locations (1)

ASST Lodi - Presidio Ospedaliero di CodognoCodogno, Lombardy, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT07665931