Hemopatch Compared to TachoSil in Postoperative Air Leak Duration After Pulmonary Resection

Air Leak From Lung Clinical Trial

Official title:
A Randomized, Controlled, Non-inferiority Study to Evaluate the Efficacy and Safety of Hemopatch Compared to TachoSil in Preventing or Reducing Postoperative Air Leaks After Pulmonary Resection

Status Completed

Clinical Trial Summary

This study is a randomized, controlled study, with the primary objective to demonstrate non-inferiority of Hemopatch compared to TachoSil in postoperative air leak duration after pulmonary resection, and with the secondary objective of evaluating the safety of Hemopatch compared to TachoSil.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Air Leak From Lung

Clinical Trial Details

NCT number	NCT03450265
Study type	Interventional
Source	Baxter Healthcare Corporation
Contact
Status	Completed
Phase	N/A
Start date	June 26, 2018
Completion date	July 9, 2019

View Details

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