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Clinical application of digital intelligent device for evaluating the effectiveness of inhaled drugs in chronic airway diseases

Clinical application of digital intelligent device for evaluating the effectiveness of inhaled drugs in chronic airway diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056579
Enrollment
Unknown
Registered
2022-02-08
Start date
2022-02-01
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

Chronic obstructive pulmonary disease, asthma

Interventions

Case group:None
Control group:None

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Normal group: no recent respiratory symptoms such as cough, sputum production and shortness of breath, no history of chronic respiratory diseases, and no abnormal pulmonary function test. 2. Asthma group: Patients met the diagnostic criteria of bronchial asthma in the Guidelines for the Prevention and Treatment of bronchial Asthma (2020 edition) and the Guidelines for the Global Initiative for the Prevention and Treatment of Asthma (2021) formulated by the Chinese Society of Respiratory Medicine, and patients in the chronic duration or clinical control period could be included with or without inhalation medication. 3. COPD group: Patients met the criteria for COPD assessment in the Guidelines for the Diagnosis and Treatment of chronic obstructive Pulmonary Disease (revised 2021) and the 2017 Global Strategy Report on the Diagnosis, Management and Prevention of Chronic obstructive Pulmonary Disease (GOLD Executive Summary) formulated by the Chinese Society of Respiratory Medicine, and inhaled drug therapy was included.

Exclusion criteria

Exclusion criteria: 1. Experimental group: (1) Failing to adopt the recommended inhalation device; (2) Patients with acute exacerbation of COPD and asthma patients with exacerbation (acute exacerbation of asthma refers to the sudden onset of wheezing, shortness of breath, cough, chest tightness and other symptoms, or exacerbation of the original symptoms, and is characterized by decreased expiratory flow, often induced by exposure to allergens, irritants or respiratory tract infection); (3) Other contraindications of pulmonary function tests; (4) Acute respiratory tract infection within four weeks. 2. Control group: (1) Patients with acute exacerbation of COPD and asthma patients with exacerbation (acute exacerbation of asthma refers to the sudden onset of wheezing, shortness of breath, cough, chest tightness and other symptoms, or exacerbation of the original symptoms, and is characterized by decreased expiratory flow, often induced by exposure to allergens, irritants or respiratory tract infection); (2) Other contraindications of pulmonary function tests; (3) Acute respiratory tract infection within four weeks.

Design outcomes

Primary

MeasureTime frame
Effective suction volume;Effective inspiratory time;Breath hold time after inhalation;Expiratory volume in first second;Exhaled nitric oxide test;ACT score;CAT score;mMRC score;Expiratory volume in the first second as a percentage of the estimated value;

Secondary

MeasureTime frame
Maximum suction flow;

Countries

China

Contacts

Public ContactGao Yi

The First Affiliated Hospital of Guangzhou Medical University

misstall2@163.com+86 13560358322

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026