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NOT YET RECRUITING
NCT06730984
NA

Endoscopy-Assisted Tracheal Intubation Versus Conventional Tracheal Intubation for Endoscopic Submucosal Dissection (ESD): a Prospective Randomized Controlled Study

Sponsor: Ningbo No. 1 Hospital

View on ClinicalTrials.gov

Summary

This study plans to enroll 148 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

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

132

Start Date

2024-12-10

Completion Date

2026-12-10

Last Updated

2024-12-12

Healthy Volunteers

No

Interventions

OTHER

Endoscopy-Assisted Tracheal Intubation

Tracheal Intubation Under Endoscopic Guidance

OTHER

Traditional Tracheal Intubation

Tracheal Intubation Under Video Laryngoscopy

Locations (1)

the First Affiliated Hospital of Ningbo University

Ningbo, Zhejiang, China