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Exhale (R) Stent for Emphysema

A Prospective Feasibility Study to Evaluate the Safety and Performance of the Exhale(R) Drug-Eluting Stent System in Patients With Emphysema

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00207337
Enrollment
60
Registered
2005-09-21
Start date
2004-07-31
Completion date
2006-05-31
Last updated
2008-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emphysema

Keywords

COPD (Chronic Obstructive Pulmonary Disease), Emphysema, Minimally invasive

Brief summary

Current treatment for emphysema is limited to measures that include inhaled oxygen, bronchodilators, anti-inflammatory drugs and pulmonary rehabilitation. Highly invasive procedures such as lung volume reduction surgery or lung transplantation are also performed. Treatment using the Exhale Drug-Eluting Stent (DES) is a minimally invasive bronchoscopic treatment that has the potential to reduce shortness of breath in emphysema patients. This study tests the safety and effects of Exhale DES in the treatment of patients with emphysema.

Detailed description

Emphysema affects an estimated 60 million people worldwide and is a major cause of morbidity and mortality. In its most basic terms, emphysema causes the destruction of lung parenchyma resulting in collateral ventilation from one part of the lung to another through the disrupted alveolar walls, to the point that gas transport from one part of the lung to another may exceed gas flow through the small airways. In other words, the gas can move freely about within the lung, but it cannot get out, which causes over inflation, or hyperinflation of the diseased lung. When the disease is far advanced, patients are afflicted with disabling dyspnea that progressively restricts their activities and eventually causes great suffering. The crippling effects of end-stage emphysema, including severe dyspnea and marked limitation of activities, relate in large measure to the dynamic hyperinflation of the lungs associated with the loss of elasticity, gas trapping and collapse of small airways. The progressive enlargement of the thorax and flattening of the diaphragm render inspiratory muscles inefficient, increase the work of breathing and contribute to a feeling of breathlessness. The major medical therapeutic modalities include bronchodilator and anti-inflammatory drugs directed at decreasing airway resistance and antibiotics to combat infection. Pulmonary rehabilitation techniques and exercise training have proven of palliative benefit. In general, the results of medical treatment for advanced airway obstruction frequently result in a persistently anguished patient and frustrated physician. A system that could efficiently decompress emphysematous lungs with each breath would result in significant clinical benefit, including lessened dyspnea, decreased work of breathing, and increased exercise tolerance. In addition to medical therapies, there are two surgical therapies available to emphysema sufferers: Lung transplantation and Lung Volume Reduction Surgery (LVRS). In the National Emphysema Treatment Trial (NETT), LVRS was shown to be effective in a sub-set of emphysema patients, but it had the drawback of increased short-term mortality as compared to the medical control arm. This was likely due to the invasiveness of LVRS. Lung transplantation is a widely accepted surgical treatment for emphysema; however it is an unrealistic option for most patients. The selection criteria are very stringent for acceptance to receive a donor lung(s). Lung transplantation carries a high long-term morbidity and mortality and is severely limited by the shortage of available donor lungs. We seek to take advantage of collateral ventilation seen in advanced emphysema by creating passageways from the lung parenchyma to large airways, through which air can escape the lungs during exhalation. The Exhale therapeutic intervention should be applicable to the majority of emphysema patients who suffer from hyperinflation of their lungs. It would be desirable to have a therapeutic option that is both less invasive and more readily available to emphysema sufferers. We have been working on such a therapy and have begun to investigate it in the clinic.

Interventions

DEVICEExhale Drug-Eluting Stent

Sponsors

Broncus Technologies
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. High resolution computed tomography (CT) scan evidence of bilateral emphysema 2. Residual volume (RV) ≥ 220% predicted. 3. Total lung capacity (TLC) ≥ 133% of predicted value. 4. Forced expiratory volume (FEV1) \< 40% of predicted or FEV1 \< 1 liter. 5. Marked dyspnea, scoring ≥ 2 on the modified Medical Research Council scale of 0-4. 6. Patient has undergone pulmonary rehabilitation of 16 - 20 sessions.

Exclusion criteria

1. FEV1 \> 20% 2. Diffusing capacity for carbon monoxide (DLco) \< 15% of predicted. 3. Respiratory infection requiring \> 3 hospitalizations in past year 4. Inability to walk \> 140 meters in 6 minutes 5. Giant bulla \> 1/3 of one lung's volume 6. Previous lung volume reduction surgery (LVRS) or lobectomy.

Design outcomes

Primary

MeasureTime frame
Procedural and technical success - operatively
Decrease in residual volume > 300mL from baseline
Safety

Secondary

MeasureTime frame
Dyspnea scoring
Quality of life measures
Pulmonary function measures
Exercise tolerance

Countries

Australia, Brazil, Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026