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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05834972
Other study ID # 34-SBKAEK-2023-05-05
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 25, 2023
Est. completion date August 10, 2023

Study information

Verified date June 2023
Source Aksaray University
Contact Cengizhan Kilicaslan, MD
Phone +905052719417
Email dr_cengizhan@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Percutaneous dilatational tracheostomy is one of the most common procedures performed in pediatric intensive care units. The investigators aimed to compare traditional landmark-guided percutaneous dilatational tracheostomy (PDT) and ultrasound-guided percutaneous dilatational tracheostomy in pediatric patients in terms of location, duration, and potential complications related to the procedure.


Description:

Tracheostomy, one of the most common procedures performed in intensive care units (ICU), refers to creating a stoma in the anterior wall of the trachea to maintain airway security. Tracheostomy can be formed via a surgical or percutaneous dilatational technique (1). The surgical technique requires the transportation of the patient to the operating theatre, while the percutaneous dilatational technique can be performed in the ICU. Thus, ICU practitioners commonly prefer the percutaneous dilatational technique. Percutaneous dilatational tracheostomy can be performed via three approaches: landmark, ultrasound (USG), or bronchoscopy guided. Although landmark-guided PTD is a practical approach, there are growing concerns regarding the location of the second and third tracheal rings and injuries to vascular structures and the thyroid gland. USG may be helpful to establish the anatomy of the airway and the vascular and glandular structure of the area. The investigators aimed to compare traditional landmark-guided percutaneous dilatational tracheostomy and USG-guided percutaneous dilatational tracheostomy in pediatric patients in terms of location, duration, and potential complications related to the procedure.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date August 10, 2023
Est. primary completion date August 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 13 Years
Eligibility Inclusion Criteria: - healthy pediatric patients - between 5 and 13 years old Exclusion Criteria: - neck anomalies - syndromic patients

Study Design


Intervention

Device:
Ultrasound-guided percutaneous dilatational tracheosyomy
All of the participants will be examined two times. First, the landmark-guided technique will be performed. Then, the ultrasound-guided technique will be performed.

Locations

Country Name City State
Turkey Aksaray University Aksaray

Sponsors (1)

Lead Sponsor Collaborator
Aksaray University

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Gobatto ALN, Besen BAMP, Cestari M, Pelosi P, Malbouisson LMS. Ultrasound-Guided Percutaneous Dilational Tracheostomy: A Systematic Review of Randomized Controlled Trials and Meta-Analysis. J Intensive Care Med. 2020 May;35(5):445-452. doi: 10.1177/0885066618755334. Epub 2018 Feb 7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Anatomical accuracy of the entry site for percutaneous dilatational tracheostomy Identification of the second and third tracheal ring 20 minutes
Secondary Detection of potential complications of the airway entry point determined by the traditional method Proximity of the airway entry point determined by the traditional method to vascular and glandular structures 20 minutes
Secondary The time taken by the landmark-guided and ultrasound-guided techniques Time taken to determine the airway entry point with landmark-guided and ultrasound-guided techniques 20 minutes
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