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Clinical Trials/NCT07236541
NCT07236541RecruitingNot Applicable

Impact of Airway Mucus Plugs on Secondary Pulmonary Fibrosis in COPD Patients: A Single-Center Case-Control Study

Ming Zhong1 site in 1 country20 target enrollmentStarted: October 30, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
20
Locations
1
Primary Endpoint
Clarify the relationship between airway mucus embolism and secondary pulmonary fibrosis in COPD patients

Study Overview

Brief Summary

Chronic obstructive pulmonary disease (COPD) is frequently accompanied by airway mucus plugs, which are closely associated with airflow obstruction, acute exacerbations, and increased mortality. However, whether mucus plugs contribute to secondary pulmonary fibrosis remains unclear. This single-center, prospective, case-control study aims to investigate the relationship between airway mucus plugs and lung fibrosis in patients with COPD undergoing lung cancer surgery.

During surgery, distal non-tumorous lung tissues and airway mucus will be collected for histological and molecular analyses. Mucus plug burden will be quantified using AB-PAS staining, and fibrosis will be assessed using Masson staining. Expression of epithelial-mesenchymal transition (EMT) markers, fibrotic markers, and the mechanosensitive ion channel Piezo1 will also be measured. COPD patients (FEV₁/FVC <0.70) will be compared with non-COPD surgical controls.

The study aims to clarify whether mucus plugs are associated with increased fibrosis and to explore the potential involvement of mechanical-signaling pathways, including Piezo1 activation. Findings may provide new clinical and pathological evidence for mucus-induced fibrotic remodeling in COPD and help identify novel therapeutic targets.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 89 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •① Age ≥ 18 years old;
  • •Planned radical resection for lung cancer, with postoperative pathological diagnosis of primary lung cancer;
  • •During surgery, non tumor lung tissue at a distance of ≥ 5 cm from the tumor edge can be obtained; ④ Case group: Preoperative pulmonary function examination confirmed diagnosis of COPD (FEV ₁/FVC<0.70); ⑤ Control group: Preoperative lung function was normal (FEV ₁/FVC ≥ 0.70), with no history of COPD; ⑥ The subjects are able to understand and sign the informed consent form

Exclusion Criteria

  • •① Clear presence of other interstitial lung diseases (ILD) or idiopathic pulmonary fibrosis before or during surgery (IPF)、 Fibrosis after pneumoconiosis or tuberculosis;
  • •Active pulmonary infections (such as bacterial pneumonia, fungal infections, active tuberculosis);
  • •Having received neoadjuvant radiotherapy or chemotherapy, which may affect the morphology or molecular results of distal lung tissue; ④ Combined severe immunodeficiency or long-term systemic immunosuppressive therapy (such as glucocorticoids ≥ 20 mg/d, More than 4 weeks);
  • •Merge with other serious systemic diseases (such as advanced heart failure, end-stage renal disease), affecting study compliance or Survival expectation; ⑥ Pregnant or lactating women; ⑦ Refusing to sign the informed consent form or deemed unsuitable by the researcher to participate in the study.

Outcomes

Primary Outcomes

Clarify the relationship between airway mucus embolism and secondary pulmonary fibrosis in COPD patients

Time Frame: At the time of surgery and within 6 months after sample collection for laboratory analysis

By comparing the distal lung tissue of patients undergoing COPD and non COPD lung cancer surgery, a systematic evaluation was conducted to determine the difference between airway mucus thrombus load and the degree of lung tissue fibrosis, and to answer whether airway mucus thrombus is an important pathological factor promoting secondary pulmonary fibrosis in COPD.

Secondary Outcomes

  • The correlation between mucus plugs and clinical features(At the time of surgery and within 6 months after sample collection for laboratory analysis)

Investigators

Sponsor
Ming Zhong
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Ming Zhong

Chief Physician and Professor, Department of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University

Shanghai Zhongshan Hospital

Study Sites (1)

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