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LVRS Versus BLVR in Patients With Homogenous Emphysema, CLUB-HE Trial

LVRS Versus BLVR in Patients With Homogenous Emphysema, CLUB-HE Trial

Non Recruiting
18-80 years
All
Phase N/A

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Overview

This is a prospective randomized clinical trial comparing surgical and bronchoscopic lung volume reduction in patients with advanced homogeneous emphysema suitable for both procedures.

Description

Lung volume reduction surgery (LVRS) as well as bronchoscopic lung volume reduction (BLVR) provide functional improvements in selected patients with homogenous emphysema and pronounced hyperinflation. A direct comparison of LVRS and BLVR in patients with homogenous emphysema is not available, thus the study will provide important data to guide treatment selection in this patient population.

Eligibility

Inclusion Criteria:

  • COPD III-IV
  • Age ≥ 18 years
  • FEV1 < 50% predicted after bronchodilatation
  • Significant hyperinflation (TLC >100% predicted, RV > 200% predicted, RV/TLC > 60%)
  • Non-smoker or ex-smoker for > 3 months (documented by cotinine testing)
  • 6 MWT >150 m and ≤ 450m
  • MRC dyspnea score > 3
  • Homogenous emphysema as assessed by HR-CT (< 15% difference in emphysema destruction score between target lobe and ipsilateral lobe) [16, 17]
  • Uni- or bilateral collateral ventilation (CV) negative result assessed fissure completeness>95% in QCT and confirmed by a bronchoscopic procedure (Chartis©)
  • Optimal medical therapy for > 3months, sufficient rehabilitation status with no need for further training/rehabilitation or rehabilitation within 6 months prior to intervention.
  • Body Mass Index (BMI) > 18, but < 35 kg/m2
  • Daily dose of prednisone ≤ 10mg

Exclusion Criteria:

  • Contraindication against either LVRS or BLVR and/or to surgery and bronchoscopy in general
  • Major comorbidities limiting survival
  • Age ≥ 80 years
  • Nicotine abuse within 3 months (documented by cotinine testing)
  • Predominance of either left or right lung of >70% in perfusion SPECT scintigraphy
  • FEV1 and/or DLCO <20% predicted (post bronchodilatation)
  • Untreated Hypoxemia (PaO2 < 50 mmHg)
  • Untreated Hypercapnia (PaCO2 > 50 mmHg)
  • Significant pulmonary fibrosis or bronchiectasis
  • Destroyed/vanished lung on HR-CT
  • Previous chest surgery or bronchoscopic interventions
  • Pulmonary hypertension (sPAP > 35 mmHg)
  • Active waiting list for lung transplantation
  • Patient is not able to understand and willing to sign a written informed consent document.
  • Pregnancy

Study details
    Emphysema or COPD

NCT04781582

Universität Duisburg-Essen

20 August 2025

FAQs

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