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Breathing Parameter Measurements for Lung Deposition Simulation

Measurement of Breathing Parameters of Asthma and COPD Patients With Different Degrees of Disease Severity for the Computer Simulation of Lung Deposition of Aerosol Drugs

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05445349
Acronym
CHOICE
Enrollment
163
Registered
2022-07-06
Start date
2022-09-01
Completion date
2025-06-30
Last updated
2025-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, COPD

Keywords

aerosol drug delivery, drug delivery optimization, inhalation therapy, breathing patterns, lung deposition modelling

Brief summary

This study aims to simulate the deposition of aerosol drugs within the airways of asthma and COPD patients based on realistic breathing patterns measured at different pulmonology centers. Further goal of the study is to find correlations between the amount of drug depositing in the lungs and the measured breathing parameters, as well as disease status and demographic data. The results of the study will be part of a major objective targeting the optimization and personalization of aerosol drug therapy.

Detailed description

The inhalation of aerosol drugs is a key element of current asthma and COPD treatment. The efficiency of the therapy is highly influenced by the dose depositing in the lungs. However, the amount of drug depositing in the lung is a result of complex drug particle-inhaler-patient interaction, thus it is inhaler-, drug- and patient-specific. Assuming that the airflow dependent aerodynamic characteristics of the drugs are known, the lung dose depends on the patient's breathing parameters during the inhalation of drug through the inhaler. In this study the inhalation parameters of asthmatic and COPD patients are measured and lung deposition assessed by a validated numerical lung deposition model. Effects of different breathing parameters (inhalation time, inhaled volume, average flow rate, peak flow rate, time until peak flow rate is reached, breath-hold time) as well as patient demographic data, disease type and disease severity on the lung dose are studied. The correlations are analysed for asthma and COPD groups separately.

Interventions

DEVICEEmptied dry powder inhalers (DPI) used in routine asthma and COPD therapy

The DPI inhaler devices are empty, without any active ingredient or/and carrier substances. Patients are not inhaling drug doses because of the study. They are inhaling only the type and quantity of aerosol drugs that they would inhale because of their treatment. The study does not influences the undergoing treatment by medication in any way.

Sponsors

Pest County Pulmonology Hospital
CollaboratorUNKNOWN
University of Debrecen
CollaboratorOTHER
St. Borbala Hospital
CollaboratorOTHER_GOV
Medical Centre Hungarian Defence Forces
CollaboratorUNKNOWN
Hospital of Komló
CollaboratorUNKNOWN
St. Pantaleon Hospital in Dunaújváros
CollaboratorUNKNOWN
Medisol Development Kft.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosed obstructive lung disease (asthma or COPD) * proper usage of inhalation tool after being educated * availability of whole body plethysmography measurement data from the last 6 months or the possibility to perform them before the start of the study * subject under outpatient/inpatient therapy * capable of acting and cooperating

Exclusion criteria

* the patient doesn't align with any of the criteria mentioned above * the patient is incapable of filling out the questionnaire/questionnaires' parts that are accorded to him/her * the patient doesn't agree to have data collected of him/her * diagnosed heavy, not treated chronic illness * not properly carried out /not evaluable lung function (spirometry) examination

Design outcomes

Primary

MeasureTime frameDescription
Lung deposition fractionJuly 1, 2023 - June 30, 2025Lung deposition fraction is the ratio of the drug dose depositing in the lungs to the dose available in the device. Lung dose will be evaluated by means of computer modelling based on input data (breathing parameters) measured in this study.

Secondary

MeasureTime frameDescription
Inhalation timeAugust 1, 2022 - June 30, 2023Inhalation time is measured while patients inhale through the empty inhalers mimicking the inhalation of aerosol drug. It expresses the duration of the inhalation in seconds.
Peak inhalation flowAugust 1, 2022 - June 30, 2023Peak inhalation flow is measured while patients inhale through the empty inhalers mimicking the inhalation of aerosol drug. It expresses the maximum value of the flow rate expressed in Liter/min.
Inhaled volumeAugust 1, 2022 - June 30, 2023Inhaled volume is measured while patients inhale through the empty inhalers mimicking the inhalation of aerosol drug. It expresses the quantity of inhaled air expressed in Liter.
Ramp-up timeAugust 1, 2022 - June 30, 2023Ramp-up time is determined from the inhalation curve measured while patients inhale through the empty inhalers mimicking the inhalation of aerosol drug. It expresses the time duration from the beginning of inhalation to the moment when the inhalation flow rate reaches its maximum value.
Breath-hold timeAugust 1, 2022 - June 30, 2023Breath-hold time is measured by the investigator and expresses the duration in seconds from the end of inhalation through the device until the beginning of exhalation.

Countries

Hungary

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026