Endotracheal Suctioning for Procedural Pain
Trial Summary
What is the purpose of 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.
Do I need to stop my current medications for this trial?
The trial protocol does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Endotracheal Tube Suctioning for procedural pain?
Is endotracheal suctioning safe for humans?
How is endotracheal tube suctioning different from other treatments for procedural pain?
Endotracheal tube suctioning is unique because it is a necessary procedure for patients on mechanical ventilation, but it is known to be painful and distressing. Unlike other treatments that might involve medication, this procedure is physical and involves removing secretions from the airway, which can cause discomfort.12345
Research Team
Elizabeth Johnston Taylor, PhD, FAAN
Principal Investigator
Loma Linda University School of Nursing
Eligibility Criteria
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.Inclusion Criteria
Exclusion Criteria
Trial Timeline
Screening
Participants are screened for eligibility to participate in the trial
Observation
Participants undergo observation with or without endotracheal tube (ETT) suctioning to assess pain and serum markers
Follow-up
Participants are monitored for changes in pain levels and serum markers post-suctioning
Treatment Details
Interventions
- Endotracheal Tube Suctioning (Procedure)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Loma Linda University
Lead Sponsor