Bio-Seal Biopsy Track Plug for Reducing Pneumothorax Rates Post Lung

Status Completed

Clinical Trial Summary

BS-1053 A Prospective Randomized Multi-Centered Safety and Efficacy Evaluation of the Bio-Seal Biopsy Track Plug for Reducing Pneumothorax Rates Post Lung Biopsy Procedures

Clinical Trial Description

This is a multi-centered, randomized trial in patients receiving lung biopsies. Patients will be randomized to either receive or not receive a Bio-Seal Biopsy Track Plug after a lung biopsy per standard hospital protocol. This study is designed to demonstrate safety and efficacy of the Bio-Seal Biopsy Track Plug in reducing pneumothorax rates post lung biopsy. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Pneumothorax

Clinical Trial Details

NCT number	NCT00562302
Study type	Interventional
Source	Angiotech Pharmaceuticals
Contact
Status	Completed
Phase	Phase 3
Start date	April 2005
Completion date	August 2008

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