Lung Volume Reduction Coils for Emphysema in Alpha-1 Antitrypsin Deficiency (LuReCAA)
Primary Purpose
Alpha-1-Antitrypsin Deficiency, Chronic Obstructive Lung Disease, Emphysema
Status
Withdrawn
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Lung Volume Reduction Coil (PneumrX Inc.)
Sponsored by
About this trial
This is an interventional treatment trial for Alpha-1-Antitrypsin Deficiency
Eligibility Criteria
Inclusion Criteria:
- Patient > 18 years of age, diagnosed with AATD emphysema
- CT scan indicates bilateral heterogeneous or non-severe homogeneous emphysema, with sufficient lung parenchyma for coil deployment, in accordance with manufacturer recommendations (see section 5.2.4.1).
- Patient has post- bronchodilator FEV1 less than or equal to 45% predicted
- Total Lung Capacity > 100%
- Residual Volume (RV) >175% predicted
- Patient has stopped smoking for a minimum of 8 weeks prior to entering the study
- Patient has read, understood and signed the Informed Consent form
- Patient is willing and able to attend all required follow-up visits
- Patient is willing and able to undergo bilateral LVRC treatment
- Patient has received Pneumococcal and Influenza vaccinations consistent with local recommendations and/or policy
Exclusion Criteria:
- Patient has a change in FEV1 > 20% post-bronchodilator.
- Patients DLCO < 20% predicted
- Patient has a history of recurrent clinically significant respiratory infection
- Patient has uncontrolled pulmonary hypertension defined by right ventricular pressure >50mmHg and or evidenced by echocardiogram
- Patient has an inability to walk >140 meters (150 yards) in 6 minutes
- Patient has evidence of other disease that may compromise survival such as lung cancer, renal failure, etc.
- Patient is pregnant or lactating
- Patient has an inability to tolerate bronchoscopy under moderate sedation or anesthesia
- Patient has clinically significant bronchiectasis
- Patient has giant bullae > 1/3 lung volume
- Patient has had previous LVR surgery, lung transplant or lobectomy
- Patient has been involved in other pulmonary drug or device studies with 30 days prior to this study
- Patient is taking > 20mg prednisone (or similar steroid) daily
- Patient is on an antiplatelet agent (such as Plavix) or anticoagulant therapy (such as heparin or coumadin) or has not been weaned off prior to procedure
- Patient has other condition that would interfere with completion of study, follow up assessments or that would adversely affect outcomes
- Patient has severe homogeneous emphysema by CT scan.
Sites / Locations
- Rigshospitalet, University of Copenhagen
- University Hospital of Saarland
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment
Arm Description
Patients with Alpha-1-Antitrypsin deficiency treated with endoscopic lung volume reduction using Lung Volume Reduction Coils (PneumRx Inc.)
Outcomes
Primary Outcome Measures
symptomatic improvement in St. George's Respiratory Questionnaire (SGRQ) from Baseline (Pre-Treatment Visit) compared to the 6 months Follow-up Visit
Quality of Life
Secondary Outcome Measures
Percent change in FEV1 from Baseline (Pre-Treatment Visit)
Lung function
Decrease in the Residual Volume and the RV/TLC ratio
Lung function
Improvement in the 6 minute walk distance
6MWT
Changes in mMRC Dyspnoe Scale
mMRC
Full Information
NCT ID
NCT02273349
First Posted
October 21, 2014
Last Updated
May 1, 2017
Sponsor
University Hospital, Saarland
1. Study Identification
Unique Protocol Identification Number
NCT02273349
Brief Title
Lung Volume Reduction Coils for Emphysema in Alpha-1 Antitrypsin Deficiency
Acronym
LuReCAA
Official Title
Evaluation of the PneumRx, Inc. Lung Volume Reduction Coil for the Treatment of Emphysema in Alpha-1 Antitrypsin Deficient Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Withdrawn
Study Start Date
October 2014 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
October 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Saarland
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objective of this study is to evaluate the safety and effectiveness of the RePneu Lung Volume Reduction Coil (LVRC) in patients with Alpha-1-Antitrypsin deficiency (AATD) caused emphysema. The hypothesis is that emphysema in AATD patients shows similar tissue destruction profile was well as symptoms and thus will respond favorably to LVRC treatment, demonstrating improvement in lung function, exercise capacity, and quality of life relative to their baseline status.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alpha-1-Antitrypsin Deficiency, Chronic Obstructive Lung Disease, Emphysema
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment
Arm Type
Experimental
Arm Description
Patients with Alpha-1-Antitrypsin deficiency treated with endoscopic lung volume reduction using Lung Volume Reduction Coils (PneumRx Inc.)
Intervention Type
Device
Intervention Name(s)
Lung Volume Reduction Coil (PneumrX Inc.)
Intervention Description
Endoscopic Lung Volume Reduction
Primary Outcome Measure Information:
Title
symptomatic improvement in St. George's Respiratory Questionnaire (SGRQ) from Baseline (Pre-Treatment Visit) compared to the 6 months Follow-up Visit
Description
Quality of Life
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Percent change in FEV1 from Baseline (Pre-Treatment Visit)
Description
Lung function
Time Frame
6 and 12 months
Title
Decrease in the Residual Volume and the RV/TLC ratio
Description
Lung function
Time Frame
6 and 12 months
Title
Improvement in the 6 minute walk distance
Description
6MWT
Time Frame
6 and 12 months
Title
Changes in mMRC Dyspnoe Scale
Description
mMRC
Time Frame
6 and 12 months
Other Pre-specified Outcome Measures:
Title
Number and type of device-related and procedure-related serious adverse events (SAE) attributed to the use of RePneu LVRC
Description
SAE device and procedure related
Time Frame
up to 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient > 18 years of age, diagnosed with AATD emphysema
CT scan indicates bilateral heterogeneous or non-severe homogeneous emphysema, with sufficient lung parenchyma for coil deployment, in accordance with manufacturer recommendations (see section 5.2.4.1).
Patient has post- bronchodilator FEV1 less than or equal to 45% predicted
Total Lung Capacity > 100%
Residual Volume (RV) >175% predicted
Patient has stopped smoking for a minimum of 8 weeks prior to entering the study
Patient has read, understood and signed the Informed Consent form
Patient is willing and able to attend all required follow-up visits
Patient is willing and able to undergo bilateral LVRC treatment
Patient has received Pneumococcal and Influenza vaccinations consistent with local recommendations and/or policy
Exclusion Criteria:
Patient has a change in FEV1 > 20% post-bronchodilator.
Patients DLCO < 20% predicted
Patient has a history of recurrent clinically significant respiratory infection
Patient has uncontrolled pulmonary hypertension defined by right ventricular pressure >50mmHg and or evidenced by echocardiogram
Patient has an inability to walk >140 meters (150 yards) in 6 minutes
Patient has evidence of other disease that may compromise survival such as lung cancer, renal failure, etc.
Patient is pregnant or lactating
Patient has an inability to tolerate bronchoscopy under moderate sedation or anesthesia
Patient has clinically significant bronchiectasis
Patient has giant bullae > 1/3 lung volume
Patient has had previous LVR surgery, lung transplant or lobectomy
Patient has been involved in other pulmonary drug or device studies with 30 days prior to this study
Patient is taking > 20mg prednisone (or similar steroid) daily
Patient is on an antiplatelet agent (such as Plavix) or anticoagulant therapy (such as heparin or coumadin) or has not been weaned off prior to procedure
Patient has other condition that would interfere with completion of study, follow up assessments or that would adversely affect outcomes
Patient has severe homogeneous emphysema by CT scan.
Facility Information:
Facility Name
Rigshospitalet, University of Copenhagen
City
Copenhagen
ZIP/Postal Code
DK-2100
Country
Denmark
Facility Name
University Hospital of Saarland
City
Homburg
State/Province
Saarland
ZIP/Postal Code
66421
Country
Germany
12. IPD Sharing Statement
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Lung Volume Reduction Coils for Emphysema in Alpha-1 Antitrypsin Deficiency
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