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Removal of Endotracheal Tube Secretions Comprehensively Until Extubation

Evaluation of the Safety and Efficacy of CAM (Complete Airway Management) Catheters: Phase II Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00663637
Acronym
RESCUE
Enrollment
30
Registered
2008-04-22
Start date
2008-04-30
Completion date
Unknown
Last updated
2008-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mechanical Ventilation, Pneumonia

Keywords

endotracheal tube obstruction, occlusion, mechanical ventilation, complication, work of breathing, airway resistance, secretions, pneumonia, ventilator associated, biofilms, endotracheal tube

Brief summary

The purpose of this study is to measure secretion accumulation within endotracheal tubes of mechanically ventilated patients and test the efficacy, safety and clinical impact of removing the secretions using novel airway management catheters (Complete Airway Management Catheters: CAM Rescue Cath and CAM Endotrach Cath).

Detailed description

Thirty mechanically ventilated adult patients will be managed with standard suction catheters. Just prior to extubation, their physiological parameters (including work of breathing) will be recorded and acoustic reflectometry used to measure the degree of secretion accumulation within the endotracheal tube. The endotracheal tubes will then be cleaned using the CAM Catheters (Rescue Cath followed by Endotrach Cath) and the physiological parameters and endotracheal tube reflectometry measurements repeated for comparative analysis.

Interventions

DEVICECAM (Complete Airway Management) Catheters

Prior to extubation, endotracheal tube lumen secretions are mechanically removed using CAM Rescue Cath followed by CAM Endotrach Cath.

Sponsors

Saint Francis Medical Center
CollaboratorUNKNOWN
Statistical Consulting
CollaboratorUNKNOWN
O. M. Neotech, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients receiving medical care in adult intensive care unit setting * Patients who have been intubated and mechanically ventilated for at least 12 hours * Patients intubated with an endotracheal tube with an internal diameter of 7.0 mm or greater

Exclusion criteria

* Patients receiving medical care in a setting not compatible with an adult intensive care unit * Patients who have been intubated and mechanically ventilated for less than 12 hours * Patients intubated with an endotracheal tube with an internal diameter of 6.5 mm or less * Patients intubated with dual lumen or steel-reinforced endotracheal tubes

Design outcomes

Primary

MeasureTime frame
work of breathingpre-extubation

Secondary

MeasureTime frame
endotracheal tube patencypre-extubation

Countries

United States

Contacts

Primary ContactRobert H. Stone, RRT
bstone@sfmc.net573-331-3000
Backup ContactStephen S. Bricknell, RRT
sbricknell@sfmc.net573-331-3000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026