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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHospital Universitari Vall d'Hebron Research Institute

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients older than 18 years

Patients undergoing surgery

Patients with predicted difficult airway

Disqualifiers

Patients under 18 years of age

Patients without cognitive disorders

Trial population

Patients older than 18 years undergoing surgery, who need fiberoptic bronchoscopy/videolaryngoscopy for tracheal intubation due to the planned difficult airway and intravenous sedation.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Sedation

    Other intervention

    Different degrees of intravenous sedation according to the Ramsay scale

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Patients intubated by fiberoptic bronchoscope1 intervention
Group B: Patients intubated by videolaryngoscopy1 intervention

Trial outcomes

Primary outcomes

1

Incidence of postperative memories

* Determine and compare, between study groups, the existence of postoperative memories according to Brice's questionnaire, in patients who need conscious tracheal intubation, under the effects of intravenous sedation. * Determine and compare, between study groups, postoperative memories for each sedation level of the Ramsay scale.

Time frame
24 hours after tracheal extubation and 30 days after

Secondary outcomes

1

Determine other adverse effects:

Record patients who present respiratory depression (SpO2 \<90%), discomfort (cough and movements)

Time frame
during fiberoptic bronchoscopy/videolaryngoscopy procedure

Other outcomes

Sponsors and contacts

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