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Procedure

Participants who undergo endotracheal tube (ETT) suctioning. for Critical Illness

N/A
Waitlist Available
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
* Adults (aged 18 years and older)
* Current diagnosis of flu, pneumonia, COVID, or sepsis
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

The goal of this experimental study is to understand if endotracheal tube (ETT) suctioning increases pain and causes stress on the body in intubated adult ICU patients. These patients are already on ventilators, which means they need suctioning to keep their airways clear, but this procedure may be uncomfortable and cause stress. The main questions this study aims to answer are: Does ETT suctioning raise pain levels as measured by the Critical-Care Pain Observation Tool (CPOT)? Does ETT suctioning increase certain chemicals in the blood (hypoxanthine, xanthine, and uric acid) that show stress and lack of oxygen in the body? Researchers will compare patients who have ETT suctioning (intervention group) with those who do not have suctioning during the study period (control group) to see if there are differences in pain and blood markers of stress. Participants will: Have pain measured before and after suctioning using the CPOT. Have blood samples taken from an existing line at three time points: 5 minutes before, 5 minutes after, and 30 minutes after suctioning. Provide demographic information (like age, gender, and diagnosis) from medical records. This research will help improve how pain is managed for ICU patients who cannot speak for themselves, potentially leading to better pain relief methods in the future.

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.
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.
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

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.

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Who is running the clinical trial?

Loma Linda UniversityLead Sponsor
316 Previous Clinical Trials
266,590 Total Patients Enrolled
Elizabeth Johnston Taylor, PhD, FAANPrincipal InvestigatorLoma Linda University School of Nursing
~73 spots leftby Apr 2025