This study plans to enroll 132 patients undergoing upper gastrointestinal endoscopic submucosal dissection (ESD). Patients will be randomly divided into a control group (conventional tracheal intubation) and an experimental group (endoscopy-assisted tracheal intubation). Patients meeting the inclusion criteria and not falling under the exclusion criteria will be invited to participate in the study. Upon providing voluntary consent, the research physician will arrange for the patient's inclusion in the study. After signing the informed consent form, the research physician will collect the patient's basic information, medical history, and other details, followed by timing the preoperative preparation period and evaluating postoperative discomfort
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
132
Tracheal Intubation Under Endoscopic Guidance
Tracheal Intubation Under Video Laryngoscopy
the First Affiliated Hospital of Ningbo University
Ningbo, Zhejiang, China
preoperative preparation time
the time from Initiate Anesthesia Induction to Insert the Therapeutic Endoscope into the Oral Cavity
Time frame: 30 minutes
The time to view the vocal cords (TVVC)
the time from inserting the tracheal tube into mouth to the operator view the the entire vocal cords
Time frame: 10 minutes
The time to advance the tracheal tube into trachea (TATT)
the time from viewing the entire vocal cords to insert the tracheal tube into trachea successfully
Time frame: 10 minutes
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