NCT04465461Completed
Video Assisted Thoracic Surgery (VATS) Fissure Completion Prior to Zephyr® Endobronchial Valve Insertion
A Pilot Study of Video Assisted Thoracic Surgery (VATS) Fissure Completion Prior to Zephyr® Endobronchial Valve Insertion for Severe Chronic Obstructive Pulmonary Disease (COPD) in Patients With COllateral VEntilation
Source: ClinicalTrials.gov · Last updated 29 Apr 2025
Brief summary (registry, in English)
Prospective, multi-centre, pilot study aimed to evaluate the effect of Video Assisted Thoracic Surgery (VATS) fissure completion on the efficacy of endobronchial valve insertion (Zephyr Valve) in the treatment of subjects with severe Chronic Obstructive Pulmonary Disease (COPD) who exhibit collateral ventilation.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 9 (actual)
- First submitted
- 7 Jul 2020
- Start date
- 4 Jun 2020
- Primary completion date
- 5 Mar 2024
- Lead sponsor
- Pulmonx Corporation
- Diseases
- COPD
- NCT number
- NCT04465461
What you commit to
- Study type: Interventional
- Participants enrolled: 9
- From 4 Jun 2020 to the primary completion date, 5 Mar 2024
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Subject has a history of previous thoracotomy, lung volume reduction surgery, prior lobectomy or pneumonectomy, prior lung transplantation, prior airway stent placement, prior pleurodesis, or prior endobronchial lung volume reduction therapy of any form.
- Subject has a history of recurrent clinically significant respiratory infections, defined as three (3) or more COPD exacerbations requiring hospitalization during the 12 months prior to study enrollment (Informed Consent Form signature page).
- Subject use of systemic steroids \> 20mg/day or equivalent and/or immunosuppressive agents in the 4 weeks prior to procedure.
- Subject is classified as having "likely" pulmonary hypertension defined as tricuspid regurgitation velocity \> 3.4m/s and/or pulmonary artery peak systolic pressure \> 45 mmHg on echocardiogram or a previous formal diagnosis of pulmonary hypertension on right heart catheterization.
Other illness
- Subject has evidence of active respiratory infection.
- Subject's pre-operative CT scan indicates the presence of any of the following radiological abnormalities:
- Pulmonary nodule ≥ 0.8 cm in diameter (does not apply if present for 2 years or more without increase in size or if proven benign by biopsy/positron emission tomography (PET)).
- Radiological picture consistent with active pulmonary infection, e.g. unexplained parenchymal infiltrate.
- Giant bullae \> 30% of the volume of either lung.
- Significant interstitial lung disease.
- Significant pleural disease.
- Subject's baseline electrocardiogram (ECG) demonstrates clinically significant arrhythmias or conduction abnormalities.
- Subject has suspected significant coronary artery disease defined as regional wall motion abnormalities on dobutamine stress echocardiogram.
- Subject is classified as being at major cardiac risk with the presence of unstable coronary syndromes (i.e. unstable or severe angina or recent myocardial infarct), decompensated heart failure, significant arrhythmias or severe valvular disease, which warrants intensive management of the condition in accordance with current guidelines on perioperative cardiovascular risk.
Other
- Subject has an acute COPD exacerbation.
- Subject has a post bronchodilator FEV1 \< 15%.
- Subject has a Diffusing capacity for carbon monoxide (DLCO) \< 20%.
- Subject has severe gas exchange abnormalities as defined by any one of the following:
- Partial pressure of oxygen (PaO2) \< 60 mmHg
- Partial pressure of carbon dioxide (PaCO2) \> 45 mmHg
- Oxygen saturation (SpO2) \< 90% on ≥ 4 L/min supplemental O2 at rest
- Subject unable to temporarily interrupt use of heparins or oral anticoagulants or antiplatelet agents, excluding aspirin.
- Clinically significant asthma (reversible airway obstruction), chronic bronchitis or bronchiectasis.
- Subject has a known diagnosis of alpha-1 antitrypsin deficiency.
Who the study is looking for
- Subject is willing and able to provide informed consent and to participate in the study.
- Subject is ≥ 40 years of age.
- Subject has a diagnosis of severe or very severe homogenous or heterogeneous COPD (Global Initiative for Obstructive Lung Disease (GOLD) classification).
- Subject has a post bronchodilator 15% ≤ FEV1 ≤ 50%.
- Subject has Total Lung Capacity (TLC) ≥ 100% predicted.
- Subject has Residual Volume (RV) ≥ 150% predicted.
- Subject has a normal dobutamine stress echocardiogram.
- Subject has sufficient exercise tolerance i.e. 150m ≤ 6MWT ≤ 450m.
- Subject has an incomplete lobar fissure i.e. \< 90%, as confirmed by CT evaluation of lung fissures.
- Collateral ventilation confirmed as assessed by Chartis Assessment (to be confirmed during first procedure/operation)
- Subject has stopped smoking for at least 8 weeks prior to entering the study as confirmed by carboxyhaemoglobin or cotinine levels.
- Subject is up to date with preventive vaccinations including seasonal influenza vaccine and pneumococcal vaccine consistent with the Victorian Department of Health and Human Services Immunization Schedule Guidelines (updated March 2018).
Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| St. Vincent's Private Hospital Fitzroy Coordinator of this site? Confirm its status | Fitzroy | Australia | Unknown status |
| St Vincent's Hospital Melbourne Coordinator of this site? Confirm its status | Fitzroy | Australia | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.