Status:
RECRUITING
BENTO - Bronchoscopic Lung Volume Reduction in Severe Emphysema Using Thermoablation
Lead Sponsor:
IHF GmbH - Institut für Herzinfarktforschung
Conditions:
Emphysema or Chronic Obstructive Pulmonary Disease
Eligibility:
All Genders
40-75 years
Phase:
NA
Brief Summary
Prospective, 2-arm, randomised (2:1), multicentre, open-label clinical trial in patients with severe emphysema. The intervention arm will be treated with Bronchoscopic lung volume reduction in severe ...
Detailed Description
Currently, there is less data on the use of bronchoscopic thermoablation (BTVA) for the treatment of patients with emphysema. However, the current studies suggest with a high degree of certainty that ...
Eligibility Criteria
Inclusion
- Age: ≥ 40 years and ≤ 75 years
- Written informed consent obtained from the patient
- Severe emphysema with indication for BTVA:
- bilateral heterogeneous emphysema of the upper lobes in GOLD stage 3/4 and
- evidence of severe emphysema in high-resolution computed tomography (not older than 6 months prior to inclusion) and
- functional evidence of severe pulmonary hyperinflation and
- FEV1 post lysis between 20% and \< 45% (calculated) and
- Total lung capacity (TLC) ≥ 100% (calculated) and
- Residual volume (RV) \> 175% (calculated) and
- arterial blood gas values of: PaCO2 ≤ 50 mmHg; PaO2 \> 50 mmHg on room air and
- marked dyspnoea with a score ≥ 2 on the Medical Research Council modified scale (mMRC) and
- 6-minute walk test \> 140 metres
- Patient-specific, pre-interventional exhaustion of conservative treatment options
- optimised medical therapy (according to the GOLD guidelines) and
- Non-smoker for 6 months prior to inclusion
- Evidence of completed pulmonary and geriatric rehabilitation in the last 4 years
- ≥ 6 weeks outpatient or
- ≥ 3 weeks inpatient or
- Individual Participation in regular physical activities that go beyond the activities of daily living (e.g. a walking programme)
- According to the investigator's assessment mentally and physically able to participate in the study procedures and visits
- Indication within the framework of an interdisciplinary case conference with specialists in pneumology, radiology and thoracic surgery in accordance with §3 of the guideline on quality assurance measures in accordance with § 136 Paragraph 1 Sentence 1 Number 2 SGB V for inpatient care with bronchoscopic lung volume reduction procedures for severe emphysema (QS-RL BLVR).
Exclusion
- Any condition that would interfere with the conduct of the clinical trial follow-up or bronchoscopy or affect the outcome of the clinical trial
- DLCO \< 20% (calculated)
- Body mass index (BMI) \< 18 kg/m2 or \> 32 kg/m2
- Pulmonary hypertension
- Peak systolic PAP \> 45 mmHg or mean PAP \> 25 mmHg
- Right heart catheter measurements are considered authoritative over echocardiogram measurements
- Clinically significant bronchiectasis
- Pneumothorax or pleural effusions within the last 6 months
- Heart and/or lung transplantation, surgical lung volume reduction (LVRS), bullectomy, lobectomy or pneumonectomy, pleurodesis or any surgery in the target lobes (upper lobes).
- Recent respiratory infection or COPD exacerbation in the last 6 weeks
- Unstable COPD (any of the following conditions):
- \>3 COPD-related hospitalisations requiring antibiotics in the last 12 months
- COPD-related hospital stay in the last 3 months
- daily use of systemic steroids, \> 5 mg prednisolone
- Single large bulla (defined as \> 1/3 of the volume of the lobe) in the upper lobe or paraseptal emphysema distribution in the lobe being treated
- Coagulopathy or current use of anticoagulants
- Patients with current endobronchial valves or with valves explanted less than 6 months ago in the target lobe in a segment to be treated with InterVapor®.
- Patients with implanted, endobronchial coils (coils)
- Patients with previous endobronchial polymer/adhesive treatment
- Patients with immune system disorders or concomitant diseases that necessitate the use of immunosuppressants of clinical relevance
- History of any of the following conditions:
- Myocardial infarction or acute coronary syndrome in the previous year
- Hospitalisation for left heart failure in the last year
- clinically leading asthma disease or alpha-1-antitrypsin deficiency
- Known sensitivity to medications required to perform bronchoscopy
- Life expectancy \< 12 months
- Newly prescribed morphine derivatives within the last 4 weeks
- Pregnancy at the time of inclusion
Key Trial Info
Start Date :
April 24 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2027
Estimated Enrollment :
224 Patients enrolled
Trial Details
Trial ID
NCT05717192
Start Date
April 24 2024
End Date
December 1 2027
Last Update
August 24 2025
Active Locations (12)
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1
Charité Campus Benjamin Franklin
Berlin, Germany, 13353
2
Gemeinschaftskrankenhaus Havelhöhe gGmbH Klinik für Anthroposophische Medizin
Berlin, Germany, 14089
3
Universitätsklinikum Bonn, Medizinische Klinik und Poliklinik II
Bonn, Germany, 53127
4
Pneumologische Universitätsklinik Ruhrlandklinik
Essen, Germany, 4542329