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Endobronchial Valve for Emphysema Palliation Trial (VENT)

Primary Purpose

Chronic Obstructive Pulmonary Disease, Emphysema

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Emphasys Endobronchial Valve and procedure
Sponsored by
Emphasys Medical
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Endobronchial Valve (EBV) Procedure, Bronchoscopic Lung Volume Reduction

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosed by high-resolution computed tomography (HRCT) with eligible heterogeneous disease distribution Forced expiratory volume in 1 second (FEV1) < 45% predicted Total lung capacity (TLC) > 100% predicted Residual volume (RV) > 150% predicted Post rehabilitation 6 minute walk test > 140m Non-smoking for 4 months Exclusion Criteria: Prior lung transplant, LVRS, median sternotomy, bullectomy or lobectomy History of recurrent respiratory infections Evidence of large bullae (>30% of either lung) in a non-target lobe FEV1 < 15% predicted Diffusing capacity for carbon monoxide (DLCO) < 20% predicted

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Pulmonary function testing at various time points through one year
    Exercise tolerance at various time points through one year
    Major complications at various time points through one year

    Secondary Outcome Measures

    Pulmonary function testing at various time points through one year
    Quality of life measures at various time points through one year
    Other adverse event rates at various time points through one year

    Full Information

    First Posted
    August 10, 2005
    Last Updated
    August 14, 2009
    Sponsor
    Emphasys Medical
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00129584
    Brief Title
    Endobronchial Valve for Emphysema Palliation Trial (VENT)
    Official Title
    Endobronchial Valve for Emphysema Palliation Trial (VENT)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2009
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2004 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Emphasys Medical

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this study is to assess the safety and efficacy of the Emphasys Endobronchial Valve (EBV) and procedure (with pulmonary rehabilitation) compared to optimal medical management (with pulmonary rehabilitation) in patients with heterogeneous emphysema.
    Detailed Description
    Background: Emphysema, caused primarily by smoking, is characterized by the gradual, irreversible breakdown of tissue and loss of elastic recoil within the lungs, causing them to lose the ability to expel air and efficiently absorb oxygen. As this chronic condition inexorably progresses, the diseased, hyperinflated areas of the lung eventually fill the chest cavity, leaving less and less volume available for the viable lung tissue. Lung volume reduction surgery (LVRS) has been shown to offer relief to patients suffering from emphysema when other treatment options fail. Researchers have continued to refine both technique and patient selection in order to improve outcomes. The objective of lung volume reduction is to eliminate dysfunctional, over-inflated regions of lung. Results similar to surgical removal have been obtained by plication (folding) and stapling without tissue removal. These results suggest that isolation of the dysfunctional lung region can achieve similar results to tissue removal. The paradoxical effect of improving lung function by removing (or isolating) lung tissue demonstrates that breathlessness due to emphysema is a function of mechanical inefficiencies in addition to loss of gas-transfer surface area and other physiological mechanisms. At least in some patients, the mechanical compromise is the primary cause of their pulmonary incapacitation and these patients can benefit by addressing their inability to effectively inhale and exhale. Because LVRS reduces trapped gas, others have speculated that results similar to LVRS could be achieved bronchoscopically by reducing the volume of the hyperinflated regions with, or without, atelectasis. Emphasys has developed a bronchoscopic approach to block inspiratory airflow into targeted, hyperinflated regions of the lung, while permitting exhaled gas to escape. This approach may lead to lung volume reduction and provide some of the clinical benefits of LVRS without the high risks and costs associated with such an invasive surgical procedure. Comparison: The primary object of this study is to assess the safety and efficacy of the Emphasys Endobronchial Valve (EBV) and procedure (with pulmonary rehabilitation) compared to medical management (with pulmonary rehabilitation) in patients with heterogeneous emphysema.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Obstructive Pulmonary Disease, Emphysema
    Keywords
    Endobronchial Valve (EBV) Procedure, Bronchoscopic Lung Volume Reduction

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    270 (false)

    8. Arms, Groups, and Interventions

    Intervention Type
    Procedure
    Intervention Name(s)
    Emphasys Endobronchial Valve and procedure
    Primary Outcome Measure Information:
    Title
    Pulmonary function testing at various time points through one year
    Title
    Exercise tolerance at various time points through one year
    Title
    Major complications at various time points through one year
    Secondary Outcome Measure Information:
    Title
    Pulmonary function testing at various time points through one year
    Title
    Quality of life measures at various time points through one year
    Title
    Other adverse event rates at various time points through one year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosed by high-resolution computed tomography (HRCT) with eligible heterogeneous disease distribution Forced expiratory volume in 1 second (FEV1) < 45% predicted Total lung capacity (TLC) > 100% predicted Residual volume (RV) > 150% predicted Post rehabilitation 6 minute walk test > 140m Non-smoking for 4 months Exclusion Criteria: Prior lung transplant, LVRS, median sternotomy, bullectomy or lobectomy History of recurrent respiratory infections Evidence of large bullae (>30% of either lung) in a non-target lobe FEV1 < 15% predicted Diffusing capacity for carbon monoxide (DLCO) < 20% predicted
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Frank C Sciurba, MD
    Organizational Affiliation
    University of Pittsburgh Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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