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EmphysemaPhase 2/3NCT00207337

Exhale (R) Stent for Emphysema

A Phase 2/3 study testing Exhale Drug-Eluting Stent in people with Emphysema, run by Broncus Technologies at 6 sites in 3 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Emphysema
What is being tested?
Exhale Drug-Eluting Stent
Type of treatment
Medical device
How many people
60 participants
Where
6 sitesin 3 countries
Study dates
Jul 2004to May 2006
Phase
Phase 2/3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

6 sites in 3 countries.

6 sites in 3 countries

Australia3 sites
  • Concord Repatriation General Hospital

    Burwood, 2134

  • The Alfred Hospital

    Prahran, Victoria, 3181

  • The Prince Charles Hospital

    Rode Road, Chermside, Queensland, 4032

Other trials in Australia

Germany2 sites
  • Medizinische Hochschule Hannover

    Hanover, 30625

  • Universitätsklinik des Saarlandes

    Homburg, Saarland, 66421

Other trials in Germany

Brazil1 site
  • Irmandade Santa Casa de Misericordia

    Porto Alegre, 90020-090

Other trials in Brazil

About this study

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

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.

Read the 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.

Conditions
Emphysema
Being tested
Exhale Drug-Eluting Stent
Keywords
COPD (Chronic Obstructive Pulmonary Disease), Emphysema, Minimally invasive
Medical subject headings
Emphysema, Pulmonary Disease, Chronic Obstructive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Exhale Drug-Eluting StentDevice

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Procedural and technical success - operatively

  2. Decrease in residual volume > 300mL from baseline

  3. Safety

Secondary outcomes (4)
  1. Dyspnea scoring

  2. Pulmonary function measures

  3. Exercise tolerance

  4. Quality of life measures

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Sep 2005 (estimated)
  2. Study startJul 2004
  3. Primary completionMay 2006
  4. Study completionMay 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
60 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00207337
Sponsor's protocol ID
0304-28
Status last verified
Jan 2008
First submitted
12 Sep 2005
Last updated
23 Jan 2008
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing Exhale Drug-Eluting Stent in people with Emphysema, run by Broncus Technologies at 6 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Jan 2008. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in Australia, Germany, Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Procedural and technical success - operatively. The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jan 2008.

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