The Effects of Endotracheal Suctioning on Pain and Serum Markers
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
- Intensive Care Unit ICU
- Intubation
- Critical Illness
- Mechanical Ventilation
- Pain Measurement
- Pain, Procedural
- Oxidative Stress
- Hypoxia
- Biomarkers / Blood
- Adult
- Uric Acid
- Sepsis
- COVID
- Influenza
- Pneumonia
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
Arm | Description | Assigned Intervention |
---|---|---|
Experimental Participants who undergo endotracheal tube (ETT) suctioning. |
Participants will receive ETT suctioning as part of routine care. |
|
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