EUROPT Clinical Trial to Study the Efficacy of One-Way Valve Implantation (New Treatment Algorithm) in Patients With Heterogeneous Emphysema

Chronic Obstructive Pulmonary Disease Clinical Trial

— EUROPT  

Official title:

A Multi-Center, Prospective, Clinical Trial Designed to Study the Efficacy of One-Way Valve Implantation Based on a New Treatment Algorithm in Patients With Heterogeneous Emphysema

Clinical Trial Details — Status: Unknown status

Administrative data

• NCT number: NCT00730301
• Other study ID #: EUROPT 07-074-0507
• Status: Unknown status
• Phase: Phase 4
• First received: August 5, 2008
• Last updated: August 5, 2008
• Start date: July 2007

Study information

• Verified date: August 2008
• Source: LudwLudwig Boltzmann Institute for COPD and Respiratory Epidemiology
• Contact: Arschang Valipour, MD
• Phone: +43-1-91060-41833
• Email: arschang.valipour[@]wienkav.at
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the efficacy of a new treatment algorithm for bronchoscopic lung volume reduction (BLVR) in patients with emphysema based on the information of emphysema heterogeneity, destruction score, and fissure analysis.

Description:

Emphysema is a progressive pulmonary disease characterized by abnormal and permanent enlargement of air spaces distal to terminal bronchioles accompanied by the destruction of pulmonary parenchyma. Treatment includes inhaled bronchodilator therapy, rehabilitation and/or oxygen treatment. In addition to the above, patients with severe emphysema may benefit from surgical lung volume reduction and/or lung transplantation. The rationale for lung volume reduction surgery is that reducing lung size would restore elastic recoil of the lung and improve chest wall and diaphragm mechanics. It has previously been shown that particularly patients with heterogeneous emphysema seem to benefit most from surgical lung volume reduction.

Bronchoscopic lung volume reduction (BLVR) has recently been introduced as a less invasive potential alternative to surgical lung volume reduction. BLVR attempts to achieve the effects of surgery, by placing bronchial prostheses using a fibreoptic bronchoscope to selectively occlude the airways supplying the most affected hyperinflated regions of the emphysematous lung, while permitting exhaled gas to escape. This attempts to achieve segmental or lobar volume reduction, simulating the effects of surgical LVR. Recent trials of BLVR using endobronchial one-way valves demonstrated significant improvements in lung function parameters, exercise capacity and quality of life in patients with end-stage emphysema. The treatment algorithm for valve implantations to achieve BLVR, however, varied considerably in these reports as well as clinical and functional response rates. Subset analysis of these studies revealed that particularly, but not exclusively, patients with radiological signs of lung volume reduction treated unilaterally showed significant clinical improvements, whereas most patients without signs of lung volume reduction did not experience these benefits. The present study investigates the response to BLVR based on a new treatment algorithm including lung function criteria and computed tomography of the thorax.

Recruitment information / eligibility

• Status: Unknown status
• Enrollment: 20
• Est. primary completion date: September 2008
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patient diagnosed by HRCT Core Lab with eligible heterogeneous disease distribution and at least one complete oblique fissure.

• Age from 40 to 75 years

• BMI < 32 kg/m2

• FEV1 < 40% of predicted value, FEV1/FVC < 70%

• TLC > 120% predicted, RV > 150% predicted.

• Stable with < 20 mg prednisone (or equivalent) qd

• PaCO2 < 50mm Hg

• PaO2 > 45 mm Hg on room air

• 6-min walk of > 50m (without rehabilitation) or > 100m (with rehabilitation)

• Nonsmoking for 4 months prior to initial interview and throughout screening

• The patient agrees to all protocol required follow-up intervals.

• The patient has no child bearing potential

• The patient is willing and able to complete protocol required baseline assessments and procedures

Exclusion Criteria:

• Prior endobronchial treatment for emphysema

• Pleural or interstitial disease that precludes surgery.

• Prior lung transplant, LVRS, median sternotomy, bullectomy or lobectomy.

• Clinically significant bronchiectasis

• Pulmonary nodule requiring surgery

• History of recurrent respiratory infections (> 3 hospitalization in the last year)

• Clinically significant (> 4 Tablespoons per day) sputum production

• Fever, elevated white cell count, or other evidence of active infection

• Dysrhythmia that might pose a risk during exercise or training

• Congestive heart failure within 6 mo and LVEF < 45%

• Evidence or history of Cor Pulmonale

• Resting bradycardia (< 50 beats/min), frequent multifocal PVCs, complex ventricular arrhythmia, sustained SVT

• History of exercise-related syncope

• MI within 6 mo and LVEF < 45%

• Evidence of systemic disease or neoplasia expected to compromise survival during 5-yr period

• Any disease or condition that interferes with completion of initial or follow-up assessments

• Patient is currently enrolled in another clinical trial

• Patient is unable to complete 3 minutes of unloaded peddling on cycle ergometer

• Alpha-1-Antitrypsin Deficiency

Related Conditions & MeSH terms

• Chronic Obstructive Pulmonary Disease
• Emphysema
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive
• Pulmonary Emphysema

Intervention

Procedure:
• Bronchoscopic Lung Volume Reduction (BLVR)
Procedure under general anesthesia.

Locations

Country	Name	City	State
Austria	Otto Wagner Hospital	Vienna
Belgium	University Antwerp	Antwerp
Belgium	University Brussels	Brussels

Sponsors (1)

Lead Sponsor	Collaborator
LudwLudwig Boltzmann Institute for COPD and Respiratory Epidemiology

Countries where clinical trial is conducted

Austria,  Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean % change in lung function (FEV1)		90 days post index bronchoscopic lung volume reduction
Secondary	Mean % change in target lobe Residual Volume and Total Lung Capacity. Mean absolute change in dyspnea (mMRC-Score), Quality of life using St. George's Respiratory Questionnaire and SF-36.		90 days post-index bronchoscopic lung volume reduction