Actively Recruiting

Age: 18Years +
All Genders
ID06514690

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients older than 18 years
  • Patients undergoing surgery
  • Patients with predicted difficult airway
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Surgery

Duration - Day of surgery

Participants undergo surgery requiring tracheal intubation using fiberoptic bronchoscopy or videolaryngoscopy under intravenous sedation.

1 surgical visit (in-person)

Post-operative Follow-up

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

Loading map...

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

Similar Trials

Comparative Study Between Combined Video Laryngoscope and Vi...

Video Laryngoscope

Actively Recruiting

1 location

Comparison of Two Sedation Regimens for Awake Fiberoptic Int...

Awake Fiberoptic Intubation

Actively Recruiting

1 location

Determination of the Incidence of Difficult Intubation and P...

Nasal Septum, Irregular

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here