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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04298814
Other study ID # COVEI
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date August 7, 2020
Est. completion date December 30, 2020

Study information

Verified date July 2020
Source Tongji Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To analyze the intubation with severe covid-19 pneumonia, the infection rate of anesthesiologist after intubation, and summarizes the experience of how to avoid the infection of anesthesiologist and ensure the safety of patients with severe covid-19 pneumonia.


Description:

To analyze the intubation time, intubation condition, intubation process, intubation times and success rate of patients with severe covid-19 pneumonia, the infection rate of anesthesiologist after intubation, the degree of respiratory improvement and survival rate of patients, and summarizes the experience of how to avoid the infection of anesthesiologist and ensure the safety of patients with severe covid-19 pneumonia.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 30, 2020
Est. primary completion date December 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Wuhan residents;

- novel coronavirus pneumonia was found to be characterized by fever and cough. Laboratory tests revealed leukocyte or lymphocyte decrease, chest CT examination showed viral pneumonia changes, and was diagnosed as COVID-19 pneumonia according to the national health and Health Committee's new coronavirus pneumonia diagnosis and treatment plan (trial version fifth Revision).

- Severe and critical patients with covid-19 pneumonia in urgent need of tracheal intubation;

- Sign informed consent.

Exclusion Criteria:

- Suspected patients with covid-19 pneumonia;

- Patients who need emergency endotracheal intubation due to other causes of respiratory failure;

- The family refused to sign the informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
severe covid-19 pneumonia with ET
severe covid-19 pneumonia undergoing endotracheal intubation

Locations

Country Name City State
China Tongji Hospital Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Tongji Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Success rate of intubation The data of Success rate of intubation with severe COVID-19 pneumonia patients the time span between 1hour before intubation and 24h after intubation
Primary Infection rate of Anesthesiologist Infection rate of Anesthesiologist who performed the endotracheal intubation for severe COVID-19 pneumonia patients the time span between 1hour before intubation and 14days after intubation
Secondary Extubation time Extubation time of intubated severe COVID-19 pneumonia patients the time span between 1hour before intubation and 30days after intubation
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