Actively Recruiting

Age: 18Years +
All Genders
NCT06514690

Postoperative Memories and Level of Sedation for Tracheal Intubation Using Fiberoptic Bronchoscopy/Videolaryngoscopy

Led by Hospital Universitari Vall d'Hebron Research Institute · Updated on 2024-08-13

100

Participants Needed

2

Research Sites

108 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Antecedentes In patients with expected difficult airways undergoing surgery, tracheal intubation must be performed with a fiberoptic bronchoscope or video laryngoscope while keeping the patient awake and under the effects of anesthetic sedation. Objective: To determine and compare the existence of postoperative memories of the patients and the different levels of sedation (Ramsay scale) obtained during the intubation procedure. Methods Prospective observational study that includes 100 patients older than 18 years who are going to undergo surgery, who need fiberoptic bronchoscopy/videolaryngoscopy for tracheal intubation due to the planned difficult airway and intravenous sedation. Patients with an unexpected difficult airway, under 18 years of age and/or with cognitive impairment will be excluded. After checking the tracheal intubation, the general anesthesia indicated for each patient will be used. Twenty-four hours after tracheal extubation, the patient will be questioned about the pain presented during the fiberoptic bronchoscopic/videolaryngoscopic procedure and postoperative memories based on a modified Brice questionnaire. At 30 days after surgery, the postoperative memories of the patients will be evaluated again by telephone interview.

CONDITIONS

Official 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

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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

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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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