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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04458220
Other study ID # SH9H-2020-T233-1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 30, 2020
Est. completion date May 30, 2025

Study information

Verified date June 2023
Source Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Contact Ren Zhou, Dr
Phone 86-15121007303
Email zhouren77@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study is performed in Shanghai Ninth People's Hospital Affiliated with Shanghai Jiao Tong University School of Medicine . According to inclusion and exclusion criteria ,the investigators are expected to enroll 16000 participants who performed endotracheal intubation under general anesthesia. All enrolled participants must sign a written informed consent.In the preset studio,The 3D face scanner and camera is used to obtain 3D or 2-dimensional portrait images of patients in different positions and from different angles.The Hi-Fi Recorder is used to obtain sound samples of patients in different word.Then,Statistical experts use quantitative software to quantify the data.The investigators will put all the data and images into a confidential database in order to build a large database of difficult airways. Anesthesiologist will give every patient an endotracheal intubation as planned. After that the anesthesiologist will be asked to fill out the questionnaire immediately.This questionnaire allows obtaining a ground truth for the intubation difficulty.All data will be used for AI deep learning and intelligent analysis,Several of the most relevant landmarks will be selected to build an early warning model.The overall study did not involve any intervention in the process of anaesthesia and operation of the patients, only the three-dimensional facial images of the patients were obtained, without any trauma or injury.


Recruitment information / eligibility

Status Recruiting
Enrollment 16000
Est. completion date May 30, 2025
Est. primary completion date May 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients to be intubated under general anesthesia. Exclusion Criteria: - Patients with deaf-mutism or communication disorders. - Patients with language deficiency or non-native language. - Patients with mental or central nervous system disease. - Patients with stupefaction or disturbance of consciousness. - Patients with terrible injury. - Patients cannot follow instructions to perform standard actions. - Patients participated in other relevant clinical investigation in the past 3 months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
photo and voice obtained
The 3D face scanner and camera is used to obtain 3D or 2-dimensional portrait images of patients in different positions and from different angles.The Hi-Fi Recorder is used to obtain sound samples of patients in different word.

Locations

Country Name City State
China The Ninth People's Hospital of Shanghai Jiaotong University School of Medicine Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnosed as a difficult airway C-L=? grade Just after intubation
Secondary Difficult mask ventilation The difficult mask ventilation was defined as follows: (1) the inability of an unassisted anesthesiologist to maintain oxygen saturation, as measured by SpO2<92% with 100% oxygen and positive-pressure mask ventilation; (2) significant gas flow leakage around the face mask; (3) the need to increase the gas flow to more than 15 L/min and use the oxygen flush valve more than twice (4) absence of visible chest movement; (5) the necessity to switch to a two-handed mask ventilation technique; (6) the need for operator substitution or addition. 2 minutes after administration of Rocuronium
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