Endobronchial Valves in Persistent Air Leak

Not Applicable

Completed

• Conditions: Malignant Neoplasm of Lung
• Interventions: Device: EndoBronchial Valve

• Registration Number: NCT01451359
• Lead Sponsor: Universitaire Ziekenhuizen KU Leuven

Brief Summary

Because an endobronchial valve is a one-way inspiratory airway blocker, it is hypothesized that it could be also used for controlling persistent air leaks while maintaining the drainage of secretions. The U.S. Food and Drug Administration approved in October 2008 the Spiration valve system designed to control air leaks in the lung that persist after lung surgery. This prospective observational study aims to evaluate the efficacy and safety of Spiration endobronchial valves in a prospective series of consecutive patients with a prolonged persistent air leak after anatomic surgical resection for cancer.

Detailed Description

Persistent Air Leak (PAL) is independently associated with prolonged hospital length of stay, decreased patient satisfaction, increased morbidity or postoperative complications, and adds significantly to the cost. The management of air leaks is primarily preventive and therefore starts in the operating room with surgical techniques that can minimize the occurrence of post-operative air leaks, such as the creation of pleural tents or use of suture line glues or sealants. Notwithstanding some patients will after a lung resection have PAL. Any minimal invasive method that helps to increase our ability to treat (reduce and/or stop) the air leak in these latest cases carries an enormous clinical as well as cost-saving potential. Bronchoscopic occlusion of a segmental or subsegmental bronchus using endobronchial valves is such a less invasive method which has shown in case reports to interrupt an air leak.

Study Timeline

• Status Verified: 2011-10
• Study Start: 2011-10
• Study First Submitted: 2011-10-04
• Study First Submitted QC: 2011-10-12
• Study First Posted: 2011-10-13
• Primary Completion: 2013-10
• Study Completion: 2013-10
• Last Update Submitted: 2013-10-08
• Last Update Posted: 2013-10-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• Prolonged (≥10 days postoperative) persistent air leak refractory to conventional treatments (such as prolonged drainage and/or chemical pleurodesis).
• Anatomical lung resection such as segmentectomy, (bi)lobectomy or sleeve lobectomy.
• Air leak after antero/posterolateral thoracotomy or video-assisted thoracoscopy (VATS).
• Type of air leak : expiratory.
• Size of air leak : any.

Exclusion Criteria

• Prolonged air leak <10 days postoperative.
• Pneumonectomy or none-anatomical lung resection.
• Lung resection for another indication than cancer.
• Previous reintervention or previous Heimlich valve for this air leak.
• Empyema

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
endobronchial valve	EndoBronchial Valve	The implantable IBV™ device is a one-way valve, designed for placement in selected regions of the bronchial tree using a flexible bronchoscope.

Primary Outcome Measures

Name	Time	Method
clinical efficacy	One month	Clinical efficacy on air leak cessation allowing drain(s) removal.

Secondary Outcome Measures

Name	Time	Method
Safety	One month	* Complications related to endobronchial valve: fever, pulmonary infection, valve migration, pneumothorax requiring treatment.; * Avoidance of ambulatory Heimlich valve and re-operation.; * Timing of drain removal.

Trial Locations

Locations (1)

University Hospitals Leuven; 🇧🇪 Leuven, Belgium