← Back to Search

Procedure

Endotracheal Suctioning for Procedural Pain

Loma Linda, CA
N/A
Recruiting
Led By Elizabeth Johnston Taylor, PhD, FAAN
Research Sponsored by Loma Linda University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Current diagnosis of flu, pneumonia, COVID, or sepsis
Intubated and receiving mechanical ventilation
Must not have
Patients receiving neuromuscular blocking agents
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change between baseline cpot score and 30-minutes post suctioning cpot score.
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to investigate if suctioning the endotracheal tube in intubated ICU patients causes pain and stress. The study will measure pain levels using a tool called CPOT and look at

See full description
Who is the study for?
This trial is for adult ICU patients who are critically ill and intubated, meaning they have a tube inserted to help them breathe. It's suitable for those with conditions like influenza, pneumonia, sepsis or COVID-19. Patients must be able to provide blood samples and have their pain assessed using the CPOT.Check my eligibility
What is being tested?
The study tests whether endotracheal tube suctioning increases pain or stress in the body by measuring changes in pain levels with the CPOT and checking blood markers before and after suctioning. Some patients will receive regular suctioning while others won't, to compare outcomes.See study design
What are the potential side effects?
While not explicitly listed, potential side effects may include discomfort from the suctioning procedure itself and possible stress response as indicated by increased levels of certain chemicals in the blood.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am currently diagnosed with flu, pneumonia, COVID, or sepsis.
 show original
Select...
I am on a breathing machine.
 show original
Select...
I have an arterial line placed.
 show original
Select...
I need a tube inserted into my windpipe to help clear it.
 show original

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I am currently taking medication for muscle control.
 show original

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change between baseline cpot score and 30-minutes post suctioning cpot score.
This trial's timeline: 3 weeks for screening, Varies for treatment, and change between baseline cpot score and 30-minutes post suctioning cpot score. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Impact of ETT suctioning on subject pain level
Impact of ETT suctioning on subject serum markers of hypoxia and oxidative stress (Hypoxanthine).

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Participants who undergo endotracheal tube (ETT) suctioning.Experimental Treatment1 Intervention
Participants will receive ETT suctioning as part of routine care.
Group II: Participants who do not undergo ETT suctioning during the observation period.Active Control1 Intervention
Participants will not receive ETT suctioning during the observation periood.

Find a Location

Closest Location:Loma Linda University Medical Center Troesh Medical Campus· Loma Linda, CA· 1117 miles

Who is running the clinical trial?

Loma Linda UniversityLead Sponsor
321 Previous Clinical Trials
267,271 Total Patients Enrolled
Elizabeth Johnston Taylor, PhD, FAANPrincipal InvestigatorLoma Linda University School of Nursing
~0 spots leftby Apr 2025