NeoMend ProGEL™ Pleural Air Leak Sealant Post-Approval Study

Status Completed

Clinical Trial Summary

The purpose of this post approval study is to further characterize the safety profile of the ProGEL™ Pleural Air Leak Sealant in commercial use, with specific reference to long-term safety over 90 days of follow-up.

Clinical Trial Description

Patients having open thoracotomy involving lung resection surgery will be considered for the study. Subjects will be examined for adverse events and complications from either the treatment or the procedure. Follow-up visits are required at 30 days and 90 days after the surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01394978
Study type	Interventional
Source	C. R. Bard
Contact
Status	Completed
Phase	N/A
Start date	June 2011
Completion date	February 2016

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