Collateral Ventilation Effects on Response to AeriSeal System Treatment in Upper Lobe Predominant Emphysema (CV+/-)
This study is currently recruiting participants.
Verified January 2012 by Aeris Therapeutics
Sponsor:
Aeris Therapeutics
Information provided by (Responsible Party):
Aeris Therapeutics
ClinicalTrials.gov Identifier:
NCT01520740
First received: January 26, 2012
Last updated: March 22, 2013
Last verified: January 2012
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Purpose
This study will evaluate the effects of baseline collateral ventilation status on outcomes following treatment with AeriSeal System in patients with advanced upper-lobe predominant heterogenous emphysema.
| Condition | Intervention | Phase |
|---|---|---|
|
Pulmonary Emphysema |
Device: Emphysematous Lung Sealant |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Collateral Ventilation Effects on Response to AeriSeal System Treatment in Upper Lobe Predominant Emphysema |
Resource links provided by NLM:
Further study details as provided by Aeris Therapeutics:
Primary Outcome Measures:
- Change from baseline in group mean post bronchodilator Forced Exhalation Volume in one second (FEV1) [ Time Frame: 24 Weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Change from Baseline in group mean 6 Minute Walk Test (6MWT) distance [ Time Frame: 24 Weeks ] [ Designated as safety issue: No ]
- Change from baseline in group mean health related quality of life [ Time Frame: 24 Weeks ] [ Designated as safety issue: No ]Change from baseline in group mean health related quality of life, measured in terms of St. George's Respiratory Questionnaire (SGRQ) total domain score
| Estimated Enrollment: | 100 |
| Study Start Date: | February 2012 |
| Estimated Study Completion Date: | August 2014 |
| Estimated Primary Completion Date: | February 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Active Comparator: Collateral Ventilation Positive (CV+) |
Device: Emphysematous Lung Sealant
4 Subsegments treated - 2 each bilaterally
Other Name: AeriSeal System Treatment
|
| Active Comparator: Collateral Ventilation Negative (CV-) |
Device: Emphysematous Lung Sealant
4 Subsegments treated - 2 each bilaterally
Other Name: AeriSeal System Treatment
|
Eligibility| Ages Eligible for Study: | 40 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Willing and able to provide informed consent and to participate in the study
- Age > or = 40 years at the time of the screening
- Advanced upper lobe predominant emphysema by CT scan
- Two (2) subsegments appropriate for treatment based upon CT scan in 2 different upper lobe segments in each lung (total 4 available subsegments)
- MRCD questionnaire score of 2 or greater at screening
- Failure of medical therapy to provide relief of symptoms
Spirometry 15 minutes after administration of bronchodilator (BOTH):
- FEV1 < 50% predicted
- FEV1/FVC ratio < 70%
Lung volumes by plethysmography (BOTH):
- TLC > 100% predicted
- RV > 150% predicted
- DLco > or = 20 and < or = 60% predicted
- Oxygen saturation (SpO2) > 90% on < or = 4 L/min supplemental O2, at rest
- Six-Minute Walk Test distance > or = 150 m
- Abstinence from smoking for at least 16 weeks prior to screening
Exclusion Criteria:
- Prior 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 type
- Requirement for ventilator support (invasive or non-invasive)
- Three (3) or more COPD exacerbations requiring hospitalization within 1 year of Screening visit or a COPD exacerbation requiring hospitalization within 8 weeks of Screening visit
- α-1 antitrypsin serum level of <80 mg/dl (immunodiffusion) or <11µmol/L (nephelometry) at Screening visit in the absence of enzyme replacement therapy. Patients with documented α-1 antitrypsin deficiency requiring replacement therapy are excluded from the study participation.
Pulmonary hypertension, defined as:
- Echocardiogram with estimated peak systolic pressure > 45 mmHg in the presence of tricuspid valve regurgitation stated in the echocardiogram report
- If the echocardiogram shows peak systolic pressure > 45 mmHg, right heart catheterization is required to rule out pulmonary hypertension, defined as peak systolic pressure > 45 mmHg or mean pressure > 35 mmHg
- Clinically significant asthma (reversible airway obstruction) or bronchiectasis
CT scan: Presence of the following radiologic abnormalities:
- Pulmonary nodule on CT scan greater that 1.0 cm in diameter (Does not apply if present for 2 years or more without increase in size or if proven benign by biopsy/PET)
- Radiologic picture consistent with active pulmonary infection, e.g., unexplained parenchymal infiltrate
- Significant interstitial lung disease
- Significant pleural disease
- Giant bullous disease (a predominant bulla > 10 cm in diameter)
- Use of systemic steroids > 20 mg/day or equivalent, immunosuppressive agents, heparins, oral anticoagulants (e.g., warfarin, dicumarol; note: antiplatelet drugs including aspirin and clopidogrel are permitted) and investigational medications within 4 weeks of screening
- Allergy or sensitivity to medications required to safely undergo AeriSeal System treatment
- Participation in an investigational study of a drug, biologic, or device not currently approved for marketing within 30 days prior to the screening visit
- 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
Significant comorbidity that carries prohibitive risks or is associated with less than 2-year expected survival, including any of the following:
- HIV/AIDS
- Active malignancy
- Stroke or TIA within 12 months of screening
- Myocardial infarction within 12 months of screening
- Congestive heart failure within 12 months of screening defined at clinical evidence of right or left hear failure or left ventricular ejection fraction < 45% on echocardiogram
- Any condition that the Investigator believes 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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01520740
Locations
| Germany | |
| Zentralklinik Bad Berka GmbH | Recruiting |
| Bad Berka, Germany, 99437 | |
| Contact: Susan Wiegand +49 0 364585-3123 studien@zentralklinik.de | |
| Principal Investigator: Reiner Bonnet, Dr. med. | |
| Charite Campus Virchow-Klinikum | Recruiting |
| Berlin, Germany, 10117 | |
| Contact: Ralf-Harto Huebner, Dr. med +49 30450 550 112 ralf-harto.huebner@charite.de | |
| Principal Investigator: Ralf-Harto Huebner, Dr. med. | |
| Klinikum Coburg | Recruiting |
| Coburg, Germany, 96450 | |
| Contact: Andrea Hohn 09561-22 7264 andrea.hoehn@klinikum-coburg.de | |
| Principal Investigator: Wolfgang Hohenforst-Schmidt, Dr. med | |
| Klinikum Donaustauf | Recruiting |
| Donaustauf, Germany, 93093 | |
| Contact: Gerlinde Hartl +49 0 9403 800 Studienzentrum@klinikum-donaustauf.de | |
| Principal Investigator: Michael Pfeifer, Dr. med | |
| Asklepios Fachkliniken Muenchen - Gauting | Recruiting |
| Gauting, Germany, 82131 | |
| Contact: Christa Niehaus c.niehaus@asklepios.com | |
| Principal Investigator: Wolfgang Gesierich, Dr. med. | |
| Universitatsklinikum Halle | Recruiting |
| Halle, Germany, 06120 | |
| Contact: Susanne Behl 0345 557 3239 susanne.behl@uk-halle.de | |
| Principal Investigator: Bernd Schmidt, Dr. med. | |
| Asklepios Klinik Hamburg-Harburg | Recruiting |
| Hamburg, Germany, 21075 | |
| Contact: Andrea Moller +49401818865016 and.moeller@asklepios.com | |
| Principal Investigator: Christoph Petermann, Dr. med. | |
| Thoraxklinik am Uniklinikum Heidelberg | Recruiting |
| Heidelberg, Germany, D-69126 | |
| Contact: Brigitte Rump +49 (0)6221 3968-211 brigitte.rump@thoraxklinik-heidelberg.de | |
| Principal Investigator: Felix Herth, MD | |
| Sana Kliniken Luebeck | Recruiting |
| Luebeck, Germany, 23560 | |
| Contact: Tahsin Balli, Dr. med +49 451 5851109 Tahsin.Balli@sana.de | |
| Principal Investigator: Tahsin Balli, Dr. med. | |
| Medizinische Klinik und Poliklinik Grosshadern | Recruiting |
| Munchen, Germany, 81377 | |
| Contact: Claus Neurohr, Dr. med. +49 89 7095 3071 Claus.Neurohr@med.uni-muenchen.de | |
| Principal Investigator: Claus Neurohr, Dr. med. | |
| Israel | |
| Hadassah - Hebrew University Medical Center | Recruiting |
| Jerusalem, Israel, 91120 | |
| Contact: Raphael Breuer +972-2-6776817 raffi@hadassah.org.il | |
| Principal Investigator: Raphael Breuer, Dr. | |
| Carmel Medical Center | Not yet recruiting |
| Petach-Tikva, Israel, 49100 | |
| Contact: Mordechai Kramer, Dr +972 0 3-9377221 kremerm@clalit.org.il | |
| Principal Investigator: Mordechai Kramer, Dr | |
| Chaim Sheba Medical Center | Not yet recruiting |
| Tel Aviv, Israel, 52621 | |
| Contact: Tiberiu Shulimzon, Dr +972 9 959220 Tiberis.Shulimzon@sheba.health.gov.il | |
| Principal Investigator: Tiberiu Shulimzon, Dr | |
Sponsors and Collaborators
Aeris Therapeutics
Investigators
| Study Director: | Janine McDermott, MS CCRP | Aeris Therapeutics |
More Information
No publications provided
| Responsible Party: | Aeris Therapeutics |
| ClinicalTrials.gov Identifier: | NCT01520740 History of Changes |
| Other Study ID Numbers: | 03-C11-004PLV |
| Study First Received: | January 26, 2012 |
| Last Updated: | March 22, 2013 |
| Health Authority: | Germany: Ethics Commission Israel: Ministry of Health |
Keywords provided by Aeris Therapeutics:
|
Gold Stage III Gold Stage IV Chronic Obstructive Pulmonary Disease COPD Lung Volume Reduction Surgery LVRS |
Bronchoscopic Lung Volume Reduction BLVR Upper Lobe Predominant ULP Heterogeneous Homogeneous |
Additional relevant MeSH terms:
|
Emphysema Pulmonary Emphysema Pathologic Processes Lung Diseases Respiratory Tract Diseases |
ClinicalTrials.gov processed this record on May 22, 2013