← Back to Search

Procedure

New Tube Type for Mechanical Ventilation (RESCUE Trial)

Phase 2

Waitlist Available

Research Sponsored by O. M. Neotech, Inc.

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Patients receiving medical care in adult intensive care unit setting

Patients who have been intubated and mechanically ventilated for at least 12 hours

Timeline

Screening 3 weeks

Treatment Varies

Follow Up pre-extubation

Awards & highlights

RESCUE Trial Summary

This trial will test if a new type of tube can help remove secretions from the lungs of people on mechanical ventilation.

Who is the study for?

This trial is for adults in intensive care who have been on a mechanical ventilator with an endotracheal tube size of 7.0 mm or larger for at least 12 hours. It's not suitable for those intubated with smaller tubes, dual lumen or steel-reinforced tubes, or patients outside adult ICU settings.Check my eligibility

What is being tested?

The study tests the effectiveness and safety of novel airway management catheters (CAM Rescue Cath and CAM Endotrach Cath) to remove secretions from the breathing tubes of patients receiving mechanical ventilation.See study design

What are the potential side effects?

Potential side effects may include discomfort during secretion removal, possible injury to the airway, and risks associated with suctioning such as changes in heart rate or oxygen levels.

RESCUE Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Select...

I am currently receiving care in an adult intensive care unit.

Select...

I have been on a breathing machine for at least 12 hours.

RESCUE Trial Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ pre-extubation

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~pre-extubation

This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-extubation for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

work of breathing

Secondary outcome measures

endotracheal tube patency

0 / 2Eligibility criteria met

Find a Location

Who is running the clinical trial?

O. M. Neotech, Inc.Lead Sponsor

Saint Francis Medical CenterUNKNOWN

Statistical ConsultingUNKNOWN

Media Library

Complete Airway Management Catheters: CAM Rescue Cath and CAM Endotrach Cath (Procedure) Clinical Trial Eligibility Overview. Trial Name: NCT00663637 — Phase 2

Pneumonia Clinical Trial 2023: Complete Airway Management Catheters: CAM Rescue Cath and CAM Endotrach Cath Highlights & Side Effects. Trial Name: NCT00663637 — Phase 2

Complete Airway Management Catheters: CAM Rescue Cath and CAM Endotrach Cath (Procedure) 2023 Treatment Timeline for Medical Study. Trial Name: NCT00663637 — Phase 2

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Has this course of medication been condoned by the FDA?

"While there is data supporting the safety of this Phase 2 treatment, none of it speaks to efficacy. Therefore, we've rated it a 2."

Answered by AI

Does this experiment still need more participants?

"The listing for this clinical trial on clinicaltrials.gov reveals that the study is not presently looking for new participants. This particular research project was first posted on April 1st, 2008 and was last edited on May 28th of the same year. There are, however, 213 other trials enrolling patients at this time."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Removal of Endotracheal Tube Secretions Comprehensively Until Extubation

2008. "Removal of Endotracheal Tube Secretions Comprehensively Until Extubation". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT00663637.

All > Missouri