Effectiveness of Reel-time Ultrasound-guided Tracheostomy and Landmark Percutaneous Dilatational Tracheostomy

August 22, 2022 updated by: HULYA TOPCU

Comparative Effectiveness of Reel-time Ultrasound-guided Tracheostomy and Anatomic Landmark Percutaneous Dilatational Tracheostomy: a Retrospective Cohort Study

This study aims to assess the impact of real-time ultrasound (US) use on complication rates and procedural success in percutaneous dilational tracheostomy (PDT) opened with forceps dilatation technique using anatomical landmarks.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study, patients who were admitted to the intensive care unit of hospital and who had a tracheostomy were examined. This is a retrospective study conducted to evaluate the method used during tracheostomy and themcomplications that occurred during and after tracheostomy opening.

2852 intensive care patients hospitalized in hospital intensive care unit after obtaining ethical permission were investigated retrospectively by scanning their files and digital data, and their complications during and after tracheostomy procedures.

Study Type

Observational

Enrollment (Actual)

1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Çorum, Turkey, 19030
        • Çorum training and research state hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients over the age of 18 who were hospitalized in the intensive care unit and underwent tracheostomy

Description

Inclusion Criteria:

  • Hospitalized in the intensive care unit and tracheostomy was opened and over 18 years.

Exclusion Criteria:

  • surgical opened tracheostomy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group G
Group G is a tracheostomy group opened using the anatomical sign technique (Griggs technique).
Other: retrospektif study; The effect of tracheostomy tecnique method on complications
retrospektif study; The effect of tracheostomy tecnique method on complications complications and correlation of complications with techniques
Group U
Group U; Ultrasound-guided is used during tracheostomy technique.
Other: retrospektif study; The effect of tracheostomy tecnique method on complications
retrospektif study; The effect of tracheostomy tecnique method on complications complications and correlation of complications with techniques

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ultrasound-guided Tracheostomy and Landmark Percutaneous Dilatational Tracheostomy
Time Frame: 01.04.2017-11.03.2019
the relationship of complications with the tracheostomy technique
01.04.2017-11.03.2019

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

HULYA TOPCU

Collaborators

Serhat Ozciftci

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2019

Primary Completion (Actual)

November 10, 2019

Study Completion (Actual)

December 22, 2021

Study Registration Dates

First Submitted

August 9, 2022

First Submitted That Met QC Criteria

August 22, 2022

First Posted (Actual)

August 24, 2022

Study Record Updates

Last Update Posted (Actual)

August 24, 2022

Last Update Submitted That Met QC Criteria

August 22, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CorumTRH

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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