Pilot Study of the Spiration IBV™ System

Emphysema Clinical Trial

Official title:

Pilot Study of the Spiration IBV™ System

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00145548
• Other study ID #: CPR-0003
• Status: Completed
• Phase: Phase 2
• First received: September 1, 2005
• Last updated: June 14, 2011
• Start date: December 2003
• Est. completion date: August 2007

Study information

• Verified date: May 2007
• Source: Spiration, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The Spiration Intra-Bronchial Valve is intended for use as a minimally invasive treatment for severe emphysema, using standard bronchoscopy. The valve is designed to limit airflow to a selected portion of the lung, producing a reduction in lung volume, which may improve pulmonary function in patients with emphysema.

Description:

This pilot study is an open enrollment, prospective study with each subject serving as their own control. The sponsor may attempt to include the data from this study in the statistical analysis of the pivotal study. This proposal shall be evaluated at the conclusion of the pilot study.

PATIENT POPULATION Patients with severe emphysema are eligible to be screened for enrollment in this study. In this initial pilot study, eligible subjects will have severe, heterogeneous, predominantly upper lobe emphysema, as defined by the American Thoracic Society (ATS) 1 and the NETT Research Group.2

These subjects also will be patients who have been screened as potential candidates for LVRS, but who have been excluded from surgical treatment due to a failure to satisfy the inclusion and exclusion criteria established by the NETT Research Group for LVRS.2 Patients also will be able to tolerate a flexible bronchoscopy procedure.

Patients who have been screened and accepted for a lung transplant procedure or LVRS, and are currently registered or scheduled for such a procedure, are not eligible for enrollment in this pilot study.

Patients with an FEV1 < 20% predicted and either homogeneous emphysema or DLCO < 20% will be excluded from enrollment in this pilot study.3

Patients will be screened and enrolled until up to 115 subjects have undergone treatment with the IBV System. Up to 15 clinical centers will be selected to enroll and treat subjects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 91
• Est. completion date: August 2007
• Est. primary completion date: August 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Male and Female subjects at least 18 years of age.

• Subject has severe, heterogeneous, predominantly upper lobe emphysema.

• Subject has ability to meet goals of, or currently satisfies goals of, a comprehensive pulmonary rehabilitation program.

• Subject has satisfied requirement for post-rehabilitation 6-minute walk of = 140 m 6 and is able to complete 3 min unloaded pedaling in exercise tolerance test.

• Subject has abstained from cigarette smoking for 4 months, as confirmed by urine or serum cotinine test.

• Pulmonary function testing results demonstrate:

• FEV1 = 45% predicted (= 15% predicted if age = 70 years)

• TLC = 100% predicted

• RV = 150% predicted

• Arterial blood gas level indicates:

• PCO2 = 50 mm Hg

• PO2 = 45 mm Hg on room air (Denver criterion: PO2 = 30 mm Hg)

• Subject has no co-existing major medical problems that would significantly increase the risk of the bronchoscopy procedure and is classified as ASA Class P4 or lower.

• If female, subject is not pregnant by a negative HCG pregnancy test within 7 days prior to the procedure.

• Subject has willingness to undertake the risk and morbidity associated with the required bronchoscopic procedures.

• Subject has willingness to participate in the study and complete the required follow-up visits.

• Subject has ability to provide informed consent.

• Subject has provided consent for treatment under this protocol and has granted access to relevant medical records to the sponsor, the Principal Investigator, the institution, the IRB and the FDA pertaining to their current lung disease condition, evaluation process, and the surgical procedure.

Exclusion Criteria:

• Patients with FEV1< 20% predicted and either homogeneous emphysema or DLCO < 20%. 3

• Subject is unable to provide informed consent.

• Subject is not an appropriate candidate for, or unable to tolerate, flexible bronchoscopy procedures.

• Subject has dysrhythmia that might pose a risk during exercise or training.

• Subject has resting bradycardia (< 50 beats/min); frequent multifocal PVCs; complex ventricular arrhythmia; sustained SVT.

• Subject has history of exercise-related syncope.

• Subject has uncontrolled hypertension (systolic, > 200 mm; diastolic > 110 mm).

• Subject has history of recurrent infections with clinically significant sputum production

• Subject has known, active asthma, chronic bronchitis or clinically significant bronchiectasis.

• Subject has giant bulla (> 1/3 volume of lung).

• Subject has pulmonary hypertension: peak systolic PPA, = 45 mm Hg (Denver criterion:

= 50 mm Hg) or mean PPA, = 35 mm Hg (Denver criterion: = 38 mm Hg). (Right heart catheter is required to rule out pulmonary hypertension if peak systolic PPA on echocardiogram is = 45 mm Hg.)

• Subject has requirement for > 6 L O2 to keep saturation = 90% with exercise.

• Subject has evidence of systemic disease or neoplasia expected to compromise survival during the 1-year study period.

• Subject demonstrates 6MWT distance = 140 m after rehabilitation.

• Subject has any disease or condition that interferes with completion of initial or follow-up assessments.

• Subject has demonstrated unwillingness or inability to complete screening or baseline data collection procedures.

• Subject has only the homogeneous emphysema pattern.

• Subject is classified as ASA Class greater than P4 7 including presence of co-morbidity that could significantly increase the risk of a standard bronchoscopy procedure.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Emphysema

Intervention

Device:
• Intra Bronchial Valve

Locations

Country	Name	City	State
United States	Emory Health Care	Atlanta	Georgia
United States	University of Alabama	Birmingham	Alabama
United States	Lahey Clinic	Burlington	Massachusetts
United States	University of Virginia Health System	Charlottesville	Virginia
United States	Cleveland Clinic Foundation	Cleveland	Ohio
United States	The Ohio State University	Columbus	Ohio
United States	Duke University Medical Center	Durham	North Carolina
United States	Indiana University	Indianapolis	Indiana
United States	North Shore - Long Island Jewish Health System	Long Island	New York
United States	Cedars-Sinai Medical Center	Los Angeles	California
United States	Columbia University Medical Center	New York City	New York
United States	University of Pennsylvania Medical Center	Philadelphia	Pennsylvania
United States	Mayo Clinic	Scottsdale	Arizona
United States	University of Washington Medical Center	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
Spiration, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary endpoint of this study is to evaluate the safety of the device, during deployment and short-term implantation for a period of up to 3 months.
Secondary	The secondary endpoint is to estimate the effectiveness achieved after 1 and 3 months of use.

External Links

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