Actively Recruiting
Post Intubation Neurologic Outcomes in Critically Ill Adults
Led by King Abdulaziz University · Updated on 2022-08-16
1000
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the impact of oxygen desaturation during emergency intubation on brain function in critically ill, non-trauma adult patients. This observational study aims to understand whether low oxygen levels during intubation affect neurological outcomes, helping guide clinical practice to reduce these risks. The brain's sensitivity to oxygen deprivation makes this an important focus, especially since emergency intubation can cause varying degrees of oxygen drop. Participants are grouped based on whether they experience hypoxia during intubation after induction but before the placement of the endotracheal tube. The study observes patients in emergency departments, critical care units, and inpatient floors undergoing emergent intubations as determined by their treating physicians. There are no investigational treatments given as this is an observational study. During the study, researchers assess neurological function using the Modified Rankin Scale up to 30 days post-intubation. They also monitor in-hospital mortality, ICU and hospital stay lengths, aspiration incidents within 14 days, and complications occurring within 24 hours of intubation. This comprehensive follow-up helps evaluate the consequences of hypoxia during emergency intubation in critically ill adults.
CONDITIONS
Brief Title
Neurologic Function Post Intubation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults older than 17 years
- Good baseline neurologic function with Modified Rankin Scale score between 1 and 3
- Undergoing emergent intubation as determined by treating physician
- Intubations occurring in emergency departments, critical care units, or inpatient floors
You will not qualify if you...
- Pediatric patients 17 years old or younger
- Pregnant patients
- Intubations occurring in the operating room
- Prisoners
- Trauma patients
- Patients with status epilepticus
- Patients with primary intracranial pathology
- Patients who had cardiopulmonary arrest
- Poor baseline neurologic function with Modified Rankin Scale score 4 or 5
- Patients intubated before hospital arrival (pre-hospital intubation)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of intubation
Participants undergo emergent endotracheal intubation and are observed for oxygen desaturation during the procedure.
1 visit (in-person)
Duration - Up to 30 days
Participants are monitored for neurologic function and other outcomes following intubation.
Follow-up visits up to 30 days post-intubation
Trial Site Locations
Total: 1 location
1
King Abdulaziz University Hospital
Jeddah, Saudi Arabia
Actively Recruiting
Research Team
A
Abdullah Bakhsh
A
Asseil Bossei
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2