Actively Recruiting
Postoperative Memories and Optimal Level of Sedation for Tracheal Intubation Using Fiberoptic Bronchoscopy/Vidolaryngoscopy in Patients With Anticipated Difficult Airway Undergoing Surgery
Led by Hospital Universitari Vall d'Hebron Research Institute · Updated on 2024-08-13
100
Participants Needed
2
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on patients with anticipated difficult airways who need tracheal intubation during surgery. It aims to determine and compare the presence of postoperative memories and sedation levels, measured by the Ramsay scale, during intubation performed with either a fiberoptic bronchoscope or a video laryngoscope. The study also explores how intubation duration and sedation depth relate to patient memories and respiratory depression risks. Patients undergoing surgery will receive tracheal intubation using fiberoptic bronchoscopy or videolaryngoscopy while awake, with intravenous sedation to ease anxiety and provide comfort. Sedation levels may vary according to the Ramsay scale as determined by the anesthesiologist. After confirming intubation, general anesthesia will be administered as per usual care. The study observes two groups based on the intubation method used. Participants will be monitored during the procedure for blood pressure, heart rate, oxygen levels, and sedation depth. Twenty-four hours after extubation, patients will be asked about pain and memories of the intubation using a modified Brice questionnaire. A follow-up telephone interview will assess memories again 30 days after surgery. The main outcome measured is the incidence of postoperative memories at these two time points, along with other adverse effects during the procedure.
CONDITIONS
Brief Title
Postoperative Memories and Level of Sedation for Tracheal Intubation Using Fiberoptic Bronchoscopy/Videolaryngoscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients older than 18 years
- Patients undergoing surgery
- Patients with predicted difficult airway
You will not qualify if you...
- Patients under 18 years of age
- Patients without cognitive disorders
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 screening and enrollment visit (in-person)
Duration - Day of surgery
Participants undergo surgery requiring tracheal intubation using fiberoptic bronchoscopy or videolaryngoscopy under intravenous sedation.
1 surgical visit (in-person)
Duration - 30 days
Participants are assessed for postoperative memories and pain 24 hours after tracheal extubation and again 30 days after surgery by telephone interview.
1 in-person visit 24 hours after extubation and 1 telephone visit at 30 days
Trial Site Locations
Total: 2 locations
1
Susana González Suárez
Barcelona, Catalonia, Spain, 08035
Actively Recruiting
2
Susana González Suárez
Barcelona, Catalonia, Spain, 08035
Actively Recruiting
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
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