Investigation of the Relationship Between the Respiratory Profile of Patients With Obstructive Pulmonary Disease and the Effectiveness of the Inhalation Therapies

Status: Recruiting
Location: See all (7) locations...
Study Type: Observational
SUMMARY

The primary aim of the OPTIPULM study is the evaluation of recorded pulmonary function curves and, based on them, the computer modelling of lung deposition for the individually used or potentially applicable inhalation drugs. The secondary aims include assessing the patients' inhalation device usage and providing recommendations for its optimization based on the recorded breathing curves and deposition calculations. The study also compares results across different flow rates and device resistances, aiming to identify the device with the highest modelled lung deposition for each patient. Understanding and Improving Inhalation Therapy in Lung Disease The OPTIPULM study looks at how well inhaled medications reach the lungs of people living with asthma or COPD (chronic obstructive pulmonary disease). It aims to improve treatment by helping doctors choose the best inhaler for each patient based on how they breathe. Every patient breathes differently, and not all inhalers work the same way. Sometimes the medicine doesn't reach deep enough into the lungs, which can make treatment less effective. This study helps doctors better understand which device works best for each individual. What happens during the study? No new treatments or changes to medication are made. Patients do a regular breathing test (like blowing into a tube). A computer program uses this breathing data to simulate how much medicine reaches the lungs with different inhalers. Doctors can then make more personalized choices for inhalation therapy. Who can take part? Adults with asthma or COPD who are able to use their inhaler correctly and complete a breathing test. What is the benefit? Although the study does not change treatments directly, it helps improve future care by identifying the best-matching inhaler for each patient. This can lead to better symptom control and fewer exacerbations.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosed obstructive pulmonary disease (asthma or COPD) confirmed by a pulmonologist.

• Proper use of inhalation device after training.

• Routine pulmonary function test performed during medical visit.

• Ambulatory (non-hospitalized) patient.

• Age over 18 years.

• Mentally competent and able to consent.

Locations
Other Locations
Hungary
Országos Korányi Pulmonológiai Intézet
NOT_YET_RECRUITING
Budapest
Csornai Margit Kórház Pulmonológiai és Allergológia Szakambulancia
NOT_YET_RECRUITING
Csorna
Debreceni Egyetem Tüdőgyógyászati Klinika
NOT_YET_RECRUITING
Debrecen
Dunakeszi-SZTK Nonprofit Kft. Tüdőgyógyászat
NOT_YET_RECRUITING
Dunakeszi
Győr-Moson-Sopron Vármegyei Petz Aladár Egyetemi Oktató Kórház
NOT_YET_RECRUITING
Győr
• Szegedi Tudományegyetem Szent-Györgyi Albert Klinikai Központ Tüdőgyógyászati Klinika
NOT_YET_RECRUITING
Szeged
Református Pulmonológiai Centrum
RECRUITING
Törökbálint
Time Frame
Start Date: 2025-01-01
Estimated Completion Date: 2025-12-30
Participants
Target number of participants: 150
Sponsors
Leads: Tradeflex Ltd
Collaborators: Medisol Development Kft.

This content was sourced from clinicaltrials.gov