Clinical Trials Logo
  1. Home
  2. Intubation Complication
  3. NCT03184246
  4. Details
NCT03184246 Clinical Trial

The Depth of Endotracheal Tube Insertion

Intubation Complication Clinical Trial

Official title:
The Depth of Endotracheal Tube Insertion - Use of Direct Laryngoscopy and Videolaryngoscopy (GlideScope), Comparison of Methods

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03184246
Other study ID # University Hospital
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 30, 2017
Est. completion date December 4, 2018

Study information
Verified date December 2018
Source University Hospital Hradec Kralove
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators suppose that direct laryngoscopy is connected with deeper insertion of endotracheal tube in comparison to videolaryngoscopy. Correction of this malposition can cause postoperative discomfort and further complications in some patients.Routine use of videolaryngoscopy could minimize these problems.

Description:

100 patients scheduled for elective neurosurgical procedures will be randomized into two groups. Patients in group A will be intubated by videolaryngoscopy (GlideScope), patients in group B by direct laryngoscopy, in both groups will be rigid stylet used. Intubation will be done under propofol anesthesia, targeted entropy 40 to 50, and deep relaxation (neuromuscular transmission target level 0). Sufentanil will be used to block tracheal reflexes. In both groups the depth of insertion of tracheal tube will be measured in the mouth corner immediately after intubation. Next day, the unpleasant sensations and complications will be recorded (sore throat, stridor, hoarseness, cough and nausea and vomiting) during control visit of patients.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date December 4, 2018
Est. primary completion date December 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- American Society of Anesthesiologists physical status I - III

Exclusion Criteria:

- postoperative ventilation, laryngeal tumors, conditions after tracheotomy or laryngeal operations, cervical spinal hernia extraction

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• GlideScope
videolaryngoscopy (GlideScope) will be used for intubation
• Direct laryngoscopy
direct laryngoscopy will be used for intubation

Locations
Country Name City State
Czechia University Hospital Hradec Kralove Hradec Kralove

Sponsors (1)
Lead Sponsor Collaborator
University Hospital Hradec Kralove

Country where clinical trial is conducted

Czechia, 

Outcome
Type Measure Description Time frame Safety issue
Primary the depth of primary insertion of tracheal tube cm in a minute after intubation
Secondary sums of manipulation with tracheal tube number 2 minutes after intubation
Secondary complications after intubation number 24 hours after surgery
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05717907 - Suction Catheter as a Guide for Nasotracheal Intubation Under General Anesthesia N/A
Completed NCT03653910 - Effect-site Concentration of Remifentanil for Double-lumen Tubes Intubation: Airtraq VS Macintosh Laryngoscope N/A
Recruiting NCT04190524 - Sonographic Assessment of Cricoid Pressure N/A
Completed NCT02359370 - The Effects of Lidocaine and Magnesium Sulphate on the Attenuation of the Hemodynamic Response to Tracheal Intubation Phase 4
Not yet recruiting NCT05036460 - Real-time Sonography in Detecting Inadvertent Esophageal Intubation Among Difficult Intubation Patients N/A
Completed NCT03992950 - Effectiveness of Cricoid and Paratracheal Pressures for Occluding Esophagus N/A
Completed NCT05502120 - A Comparison of Vie-Scope and Macintosh Blade Laryngoscopes in Morbidly Obese. N/A
Completed NCT05303948 - Evaluation of Two Positions for Free Floating Tracheal Intubation in Weightlessness N/A
Completed NCT03720093 - Exploratory Analysis of Pulmonary Microbiome in Intubated Patients
Recruiting NCT03031808 - Comparison of Two Induction Regimens Using Topical Lidocaine or Muscle Relaxant on Sore Throat and Hemodynamics Phase 4
Not yet recruiting NCT02918526 - Hemodynamic Study With PRAM of the Cardiovascular Response to the Positioning of the Extraglottic Device N/A
Completed NCT02364622 - The Effects of Flexible Intubating Stylet in the Accurate Placement of Double-lumen Endobronchial Tube N/A
Completed NCT05249738 - Tongue Edema Caused by Intubation Tube in Intensive Care Unit Patients
Terminated NCT03340207 - Novel Airway Device to Aid Endotracheal Intubations N/A
Completed NCT03842306 - End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients
Recruiting NCT05782517 - I-gel vs. Endotracheal Intubation for Laparoscopic Gynaecological Procedures N/A
Recruiting NCT06085326 - Smart Checklist Implementation for Pediatric Tracheal Intubations in the ICU- Multicenter Study N/A
Active, not recruiting NCT06108271 - Innovative Endotracheal Tube Design Reduces Postoperative Laryngeal Injury N/A
Completed NCT05668299 - Determining the Appropriate Setting of an Automated Secretion Removal Technology (TrachFlush) N/A
Completed NCT04079387 - Effect of Endotracheal Tube Plus STYLET Versus Endotracheal Tube Alone N/A