The Effect of Different Fiberoptic Outer Diameters on Fiberoptic Intubation

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorQinye Shi

About this trial

Fiberoptic intubation is an important method for anesthesiologists to deal with difficult airways, but its operation is difficult and requires repeated practice. Fiberoptic intubation is performed in two steps. First, the anesthesiologist holds the bronchoscope and exposes the base of the tongue, the epiglottis, and the glottis successively according to the front camera of the bronchoscope. Through the glottis, the main trachea is exposed to the carina. This process is visual and the anesthesiologist can see the main tissue structure directly. Then, the endotracheal catheter enters the endotracheal along the bronchoscope, and the process of endotracheal catheter entry is not visual.

In clinical work, it was found that the tracheal catheter was easily blocked when it passed through the glottis, and it was necessary to adjust the position of the tracheal catheter for several times before the tracheal catheter could be sent into the tracheal tube, which was easy to cause throat injury in the process. At present, relevant studies are mainly focused on the first step of bronchoscopic intubation, how to quickly expose the glottis and complete the bronchoscopic guidance process. However, there is no clear mention of the situation of catatoning in the process of endotracheal catheter and how to solve the problem of catatoning.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

Limited mouth opening

limited movement of temporomandibular joint

abnormal glottic anatomy

polyps of vocal cords

Trial population

Patients in need of oral tube intubation and general anesthesia in our hospital for elective surgery

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • fiberoptic

    Device

    Tracheal intubation was performed with different outer diameters of fiberoptic.

Treatment groups

75 Participants
are divided into 3 treatment groups
Group A: 3.8mm Group1 intervention
Group B: 2.8 mm group1 intervention
Group C: 4.8mm group1 intervention

Trial outcomes

Primary outcomes

1

Fiberoptic intubation attempts

This is used to observe the passage of the tracheal tube through the glottis

Time frame
during the procedure
2

First intubation success rate

The incidence of tracheal tube through the vocal cords

Time frame
during the procedure
3

Fiberoptic intubation time

The duration of the intubation process

Time frame
during the procedure
4

Time of passage of tracheal intubation through glottis

The time the tracheal tube enters the trachea

Time frame
during the procedure

Secondary outcomes

1

Hoarseness after surgery

Patients were asked about voice changes 24 hours after surgery

Time frame
24 hours after surgery
2

Sore throat

Patients were asked about throat pain 24 hours after surgery

Time frame
24 hours after surgery

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Qinye Shi

Lead sponsor

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Sponsor institution

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