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Percutaneous Dilatation Tracheostomy, Broncoscopy, Pro-seal Laryngeal Mask

Not Applicable
Completed
Conditions
Tracheostomy Complication
Registration Number
NCT04637932
Lead Sponsor
Eylem Yaşar
Brief Summary

In this study, our primary goal is to compare whether there is any difference in the complication of using pro-seal laryngeal mask or intubation tube in bronchoscopy-guided percutaneous dilation tracheostomy procedure. Our secondary goal is to compare in terms of processing time.

Detailed Description

Following the approval of Muğla Sıtkı Koçman University Clinical Research Ethics Committee, 61 cases over the age of 18 who were scheduled for elective percutaneous dilatation tracheostomy in intensive care units were included in the study.

Elective percutaneous dilatation tracheostomy cases were randomly divided into two groups. Group 1 was determined as endotracheal tube and group 2 as pro-seal laryngeal mask group.

In the endotracheal tube group, which is a conventional method, after entering the trachea with percutaneous technique, the intubation tube was removed before dilatation and percutaneous dilatation tracheostomy was performed with the Seldinger method.

In the pro-seal laryngeal mask group, the fiberoptic bronchoscope was advanced with a pro-seal laryngeal mask, and after the correct position was achieved, percutaneous dilatation tracheostomy was performed using the Seldinger Method.

Arterial blood pressure, oxygen saturation, heart rate, arterial blood gas, mechanical ventilation mode, positive end expiratory pressure and mean airway pressure values were recorded before and 30 minutes after the procedure.

The time until the end of the procedure and complications were determined.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
61
Inclusion Criteria

hospitalized in intensive care units of our hospital and planned for elective percutaneous dilatation tracheostomy were included in the study.

Exclusion Criteria
  • history of cervical trauma,
  • high-pressure mechanical ventilation (inspiratory pressure above 40 cmH2O),
  • pulmonary edema,
  • acute respiratory distress

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
complication of percutan dilatation tracheostomy procedure.7 days

blood gas analysis, physical examination, lung auscultation, hemodynamics parameters

Secondary Outcome Measures
NameTimeMethod
processing time.minutes

Our secondary goal is to compare in terms of processing time.

Trial Locations

Locations (1)

Mugla Sitki Kocman University

🇹🇷

Mugla, Turkey

Mugla Sitki Kocman University
🇹🇷Mugla, Turkey

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