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RECRUITINGINTERVENTIONAL

The Effects of Endotracheal Suctioning on Pain and Serum Markers

The Impact of Endotracheal Suctioning on Pain, Hypoxia, and Oxidative Stress Biomarkers in Intubated Adult ICU Patients: A Controlled Trial

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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 May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - Patients receiving neuromuscular blocking agents - Contraindications for blood draws (hemoglobin levels below 8.0 g/dL; Jehovah's Witness) Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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)

Treatments Being Tested

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.

Locations (1)

Loma Linda University Medical Center Troesh Medical Campus
Loma Linda, California, United States