Refractory Breathlessness in COPD

ConditionCOPD
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorSeoul National University

About this trial

This study aims to investigate the prognosis and clinical outcomes of patients with chronic obstructive pulmonary disease (COPD) who continue to experience refractory dyspnea despite treatment with long-acting beta-agonist (LABA) and long-acting muscarinic antagonist (LAMA). The research will prospectively follow a cohort of patients to identify clinical factors, lung function parameters, imaging features, and cardiovascular indicators associated with poor treatment response. By comparing these patients with those who show symptom improvement, the study seeks to determine predictors of exacerbations, lung function decline, and mortality. Findings are expected to guide the development of targeted strategies to improve the management of refractory dyspnea in COPD.

Eligibility criteria

Qualifiers

Presence of COPD risk factors (e.g., smoking history, occupational exposure, genetic predisposition).

Typical symptoms such as dyspnea, cough, or sputum production.

Post-bronchodilator FEV1/FVC < 0.70.

Regular outpatient follow-up at the respiratory clinic.

Disqualifiers

Poor adherence to LABA/LAMA therapy (medication possession rate < 50%) or refusal of treatment.

Inability or unwillingness to comply with scheduled visits, examinations, or follow-up procedures.

End-stage diseases with life expectancy < 1 year.

Terminal malignancies receiving hospice or palliative care.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

730 Participants
are grouped into 1 trial group

Sponsors and collaborators