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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05739318
Other study ID # 2022A123
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 15, 2023
Est. completion date August 3, 2023

Study information

Verified date February 2023
Source The First Hospital of Qinhuangdao
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The comparison of the diameter of double-lumen tube at the cuff of endotracheal and endobronchial during the cuff was collapse or inflated as a guide for the selection of the size of double-lumen tube.


Description:

The comparison of the diameter of double-lumen tube at the cuff of endotracheal and endobronchial during the cuff was collapse or inflated as a guide for the selection of the size of double-lumen tube.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 3, 2023
Est. primary completion date July 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: BMI less than 35 kg/m2 ASA classifications of I-III, Modified Mallampati classification 1 or 2 Under general anesthesia Exclusion Criteria: Age younger than 18 yr or older than 70 yr - ASA class IV or V - Abnormalities of the heart, brain, liver, lung, kidney and coagulation function

Study Design


Related Conditions & MeSH terms

  • Therapeutic Procedural Complication

Intervention

Device:
The cuff of endotracheal and endobronchial is collapsed
The diameter of double-lumen tube at the cuff of endotracheal and endobronchial when the cuff is collapsed as the diameter of double-lumen tube and select a double-lumen tube that matches the patient's trachea and bronchial innerdiameter based on this diameter
The cuff of endotracheal and endobronchial is inflated
The diameter of double-lumen tube at the cuff of endotracheal and endobronchial when the cuff is inflated as the diameter of double-lumen tube and select a double-lumen tube that matches the patient's trachea and bronchial innerdiameter based on this diameter

Locations

Country Name City State
China The first hospital of Qinhuangdao Qinhuangdao Hebei

Sponsors (1)

Lead Sponsor Collaborator
The First Hospital of Qinhuangdao

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of complications Incidence of postoperative hoarseness and throat pain in patients 12 weeks
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