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Removal of Endotracheal Tube Secretions Comprehensively Until Extubation

NCT00663637 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2008-05-29

No results posted yet for this study

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).

Conditions

Interventions

DEVICE

CAM (Complete Airway Management) Catheters

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

Sponsors & Collaborators

  • Saint Francis Medical Center

    collaborator UNKNOWN

  • Statistical Consulting

    collaborator UNKNOWN

  • O. M. Neotech, Inc.

    lead INDUSTRY

Principal Investigators

  • Orlando V. Morejon, MD · Saint Francis Medical Center; Omneotech

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00663637 on ClinicalTrials.gov