Status and phase
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About
The purpose of this study is to demonstrate the safety and efficacy of AeriSeal System treatment plus optimal medical therapy compared in patients with advanced upper lobe predominant (ULP) heterogeneous emphysema.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Willing and able to provide informed consent
Age ≥ 40 years
On optimal medical therapy* for more than 1 month
Advanced upper lobe predominant emphysema confirmed by CT scan
Two (2) subsegments appropriate for treatment in 2 different upper lobe segments in each lung based upon CT scan (total 4 available subsegments)
MRCD score of ≥ 2 post pulmonary rehab (using modified MRCD scale of 0-4)
6MWT distance ≥ 150 m post pulmonary rehab
Spirometry 15 minutes after administration of a bronchodilator showing BOTH:
Plethysmographic lung volumes showing BOTH:
DLco ≥ 20% and ≤ 60% predicted
Blood gases and oxygen saturation showing BOTH:
Smoking history of ≥ 20 pack-years with abstinence for 16 weeks
Exclusion criteria
Prior lung volume reduction surgery, lobectomy or pneumonectomy, or lung transplantation
Requirement for ventilator support (other than CPAP or BPAP for sleep apnea)
Three (3) or more COPD exacerbations requiring hospitalization within 1 year of Screening visit or a COPD exacerbation requiring hospitalization within 8 weeks
Use of systemic steroids > 20 mg/day or equivalent immunosuppressive agents, heparins, oral anticoagulants or investigational medications
Exclusion Criteria (continued):
a-1 antitrypsin serum level of < 80 mg/dL (immunodiffusion) or < 11 µmol/L (nephelometry)
CT scan: Presence of any of the following radiologic abnormalities:
Clinically significant asthma
Clinically significant bronchiectasis
Pulmonary hypertension
Allergy or sensitivity to medications required to safely perform AeriSeal System treatment under general anesthesia or conscious (moderate procedural) sedation
Participation in an investigational study of a drug, biologic, or device not currently approved for marketing
Body mass index < 15 kg/m2 or > 35 kg/m2
Female patient pregnant or breast-feeding or planning to be pregnant in the next year
Any abnormal screening laboratory test result
Significant comorbidity including any of the following:
Any condition that would interfere with the intent of the study or would make participation not in the best interest of the patient such as alcoholism, high risk for drug abuse or noncompliance in returning for follow-up visits
Primary purpose
Allocation
Interventional model
Masking
300 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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