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.
Official Title
A Prospective Feasibility Study to Evaluate the Safety and Performance of the Exhale(R) Drug-Eluting Stent System in Patients With Emphysema
Conditions
Emphysema
Study Type
Interventional
Study Design
Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Further Details
Primary Outcome Measures:
- Procedural and technical success – operatively
- Decrease in residual volume > 300mL from baseline
- Safety
Secondary Outcome Measures:
- Dyspnea scoring
- Pulmonary function measures
- Exercise tolerance
- Quality of life measures
Study Start
July 2004; Study completion: May 2006
Eligibility & Criteria
- Ages Eligible for Study: 18 Years – 80 Years
- Genders Eligible for Study: Both
Inclusion Criteria:
- 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 litre.
- Marked dyspnea, scoring >= 2 on the modified Medical Research Council scale of 0-4.
- Patient has undergone pulmonary rehabilitation of 16 – 20 sessions.
Exclusion Criteria:
- 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.
Total Enrolment
60
Contact Details
- Concord Repatriation General Hospital, Burwood, 2134, Australia
- The Prince Charles Hospital, Rode Road, Chermside, Queensland, 4032, Australia
- The Alfred Hospital, Prahran, Victoria, 3181, Australia
Broncus Technologies, Inc web page
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