Clinical Trial

CeraShieldâ„¢ Endotracheal Tube Feasibility Study

Study Description

CeraShieldâ„¢ Endotracheal Tube Feasibility Study

Single-arm, feasibility study to evaluate the Ceragenin Coated Endotracheal Tube (the CeraShield ETT) in adults who require intubation and are expected to be mechanically ventilated for a?Y 24 hours.

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Recruiting patients only Recruiting patients only

Device - CeraShield Endotracheal Tube

Subjects requiring mechanical ventilation with be intubated with the CeraShield ETT

Additional Information

Official Study Title

CeraShieldâ„¢ Endotracheal Tube Feasibility Study

Clinical Trial ID

NCT03716713

ParticipAid ID

elYp6a