Purpose

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.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adults (aged 18 years and older) - Current diagnosis of flu, pneumonia, COVID, or sepsis - Intubated and receiving mechanical ventilation. - Have arterial lines placed - Require endotracheal suctioning as part of their care

Exclusion Criteria

  • Patients receiving neuromuscular blocking agents - Contraindications for blood draws (hemoglobin levels below 8.0 g/dL; Jehovah's Witness)

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Supportive Care
Masking
Single (Investigator)
Masking Description
The lab technician who results the labs will be blinded.

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Participants who undergo endotracheal tube (ETT) suctioning.
Participants will receive ETT suctioning as part of routine care.
  • Procedure: endotracheal tube suctioning
    Endotracheal tube suctioning occurs as part of normal care for intubated patients. This procedure will serve as the painful procedure to assess CPOT and biomarkers of hypoxia and oxidative stress.
No Intervention
Participants who do not undergo ETT suctioning during the observation period.
Participants will not receive ETT suctioning during the observation periood.

Recruiting Locations

More Details

NCT ID
NCT06692400
Status
Not yet recruiting
Sponsor
Loma Linda University

Study Contact

Briana Carr, PhD(c), BSN, RN
909-558-4000
bmcarr@llu.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.