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NCT04447638 Clinical Trial

Percutaneous Tracheostomy With COVID-19

Tracheostomy Clinical Trial

Official title:
Percutaneous Tracheostomy With Aerosol Box in COVID-19 Positive Patients in Intensive Care Unit: a Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04447638
Other study ID # TT17
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 20, 2020
Est. completion date June 1, 2020

Study information
Verified date September 2020
Source Çanakkale Onsekiz Mart University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Coronavirus disease 2019 (COVID-19) has brought about a requirement of intensive care and mechanical ventilation for a significant portion of patients. Percutaneous tracheostomy is performed in order to reduce the complications that may develop due to prolonged endotracheal intubation.

Description:

Different methods are needed for situations in which the potential for producing aerosols is high, such as intubation and tracheostomy. One of these methods is the aerosol box.To share our experiences of percutaneous tracheostomy performed with aerosol box in COVID-19 patients. Patients who underwent percutaneous tracheostomy between March 2020 and June 2020 in the pandemic intensive care unit were evaluated retrospectively.The study is designed as a clinical trial study. This study was performed in faculty of medicine hospital's intensive care unit which is located in Canakkale province Turkey.

Recruitment information / eligibility
Status Completed
Enrollment 24
Est. completion date June 1, 2020
Est. primary completion date June 1, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- who underwent percutaneous tracheostomy with COVID-19(+)

Exclusion Criteria:

- Patients who do not give informed consent or do not want to participate in the study

- Coagulopathy, thrombocytopenia

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Tracheostomy with aerosol box in COVID-19 positive patients
Patients who underwent percutaneous tracheostomy with aerosol box in COVID-19 positive patients. The patients age, gender, hospitalization diagnosis, number of intubated days, anesthetic agents used during the procedure, neck ultrasonography data before and during the procedure, and complications were recorded.

Locations
Country Name City State
Turkey Canakkale Onsekiz Mart University Canakkale

Sponsors (1)
Lead Sponsor Collaborator
Çanakkale Onsekiz Mart University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Complications observed in the cases in which we applied percutaneous tracheostomy with aerosol box Complications During the procedure
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