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Effect of Endotracheal Tube Plus STYLET Versus Endotracheal Tube Alone (STYLETO)

Primary Purpose

Intubation Complication, Critically Ill

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
ENDOTRACHEAL TUBE + STYLET
ENDOTRACHEAL TUBE ALONE
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intubation Complication

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients must be present in the intensive care unit (ICU) and require mechanical ventilation through an orotracheal tube.
  • Adult (age ≥ 18 years)
  • Subjects must be covered by public health insurance
  • Written informed consent from the patient or proxy (if present) before inclusion or once possible when patient has been included in a context of emergency.

Exclusion Criteria:

  • Refusal of study participation or to pursue the study by the patient
  • Pregnancy or breastfeeding
  • Absence of coverage by the French statutory healthcare insurance system
  • protected person
  • intubation in case of cardio circulatory arrest
  • Previous intubation during the same ICU stay and already included in the study

Sites / Locations

  • Centre Hospitalier Universitaire Montpellier, Saint Eloi

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

ENDOTRACHEAL TUBE + STYLET

ENDOTRACHEAL TUBE ALONE

Arm Description

The experimental group consists in intubating the trachea with an endotracheal tube + stylet with a "straight-to-cuff" shape and a bend angle of 25° to 35°.

The control group consists in intubating the trachea with an endotracheal tube alone (i.e, without stylet).

Outcomes

Primary Outcome Measures

Number of patients with successful first-pass orotracheal intubation
the proportion of patients with successful first-pass orotracheal intubation

Secondary Outcome Measures

Complications related to intubation
severe hypoxemia defined by lowest oxygen saturation (SpO2) < 80 %, severe cardiovascular collapse, defined as systolic blood pressure less than 65 mm Hg recorded at least once or less than 90 mm Hg lasting 30 minutes despite 500-1,000 ml of fluid loading (crystalloids solutions) or requiring introduction or increasing doses by more than 30% of vasoactive support, cardiac arrest, death during intubation; moderate: difficult intubation, severe ventricular or supraventricular arrhythmia requiring intervention, oesophageal intubation, agitation, pulmonary aspiration, dental injuries

Full Information

First Posted
August 29, 2019
Last Updated
December 22, 2021
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT04079387
Brief Title
Effect of Endotracheal Tube Plus STYLET Versus Endotracheal Tube Alone
Acronym
STYLETO
Official Title
Effect of Endotracheal Tube Plus STYLET Versus Endotracheal Tube Alone on Successful First-Pass Orotracheal Intubation Among Critically Ill Patients: the Randomised STYLETO Study Protocol"
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
October 1, 2019 (Actual)
Primary Completion Date
March 17, 2020 (Actual)
Study Completion Date
June 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients admitted to Intensive Care Units (ICU) often require respiratory support. Orotracheal intubation is one of the most frequent procedures performed in ICU.When performed in emergency settings, intubation is a challenging issue as it may be associated with life-threatening complications in up to one third of cases Using a preshaped endotracheal tube plus stylet may have potential advantages over endotracheal tube alone without stylet. The stylet is a rigid but malleable introducer which fits inside the endotracheal tube and allows for manipulation of the tube shape; usually into a hockey stick shape, to facilitate passage of the tube through the laryngeal inlet. The stylet can help to increase success of intubation in operating rooms
Detailed Description
Patients admitted to Intensive Care Units (ICU) often require respiratory support. Orotracheal intubation is one of the most frequent procedures performed in ICU. When performed in emergency settings, intubation is a challenging issue as it may be associated with life-threatening complications in up to one third of cases.Severe hypoxaemia occurring during intubation procedure can result in cardiac arrest,cerebral anoxia, and death.Difficult intubation is known to be associated with life-threatening complications both in operating room and in emergent conditions.ICU intubation conditions are worse than intubation conditions in operative rooms.A non-planned and urgent intubation procedure, severity of patient disease and ergonomic issues explain the morbidity associated with intubation in ICU.To prevent and limit the incidence of severe hypoxemia following intubation and its complications, several intubation algorithms have been developed ,and specific risk factors for difficult intubation in ICU have been identified. In 2018, a large multicenter study reported first-attempt intubation success rates using direct laryngoscopy of 70% and videolaryngoscopy of 67%. In 2019, a multicentre randomized trial,assessing whether positive-pressure ventilation with a bag-mask device (bag-mask ventilation) during tracheal intubation of critically ill adults prevents hypoxemia, reported a first-attempt success rate of 81%. Other authors reported an overall first-attempt intubation success rate of 74%. The 20% to 40% first-attempt failure rates throughout studies highlight the opportunity to improve the safety and efficiency of this critical procedure. Using a preshaped endotracheal tube plus stylet may have potential advantages over endotracheal tube alone without stylet. The stylet is a rigid but malleable introducer which fits inside the endotracheal tube and allows for manipulation of the tube shape; usually into a hockey stick shape, to facilitate passage of the tube through the laryngeal inlet. The stylet can help to increase success of intubation in operating rooms. However, some complications from intubating stylets have been reported including mucosal bleeding, perforation of the trachea or esophagus, and sore throat. In 2018, one study has assessed the effect of adding a stylet in case of difficult intubation in prehospital setting.However, in ICU, the systematic use of a stylet is still debated and recent recommendations do not recommend to use or not to use such devices for first-pass intubation. The device chosen for intubation may therefore be a confounding factor between the relation of stylet use and first-attempt success.The routine use of a stylet for first-pass intubation using laryngoscopes in ICU has never been assessed and benefit remains to be established. The investigators hypothesis that adding stylet to endotracheal tube will increase the frequency of successful first-pass intubation compared with use endotracheal tube alone (i.e, without stylet) in ICU patients needing mechanical ventilation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intubation Complication, Critically Ill

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1040 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ENDOTRACHEAL TUBE + STYLET
Arm Type
Experimental
Arm Description
The experimental group consists in intubating the trachea with an endotracheal tube + stylet with a "straight-to-cuff" shape and a bend angle of 25° to 35°.
Arm Title
ENDOTRACHEAL TUBE ALONE
Arm Type
Active Comparator
Arm Description
The control group consists in intubating the trachea with an endotracheal tube alone (i.e, without stylet).
Intervention Type
Device
Intervention Name(s)
ENDOTRACHEAL TUBE + STYLET
Intervention Description
The experimental group consists in intubating the trachea with an endotracheal tube + stylet with a "straight-to-cuff" shape and a bend angle of 25° to 35°
Intervention Type
Device
Intervention Name(s)
ENDOTRACHEAL TUBE ALONE
Intervention Description
intubating the trachea with an endotracheal tube alone
Primary Outcome Measure Information:
Title
Number of patients with successful first-pass orotracheal intubation
Description
the proportion of patients with successful first-pass orotracheal intubation
Time Frame
At intubation
Secondary Outcome Measure Information:
Title
Complications related to intubation
Description
severe hypoxemia defined by lowest oxygen saturation (SpO2) < 80 %, severe cardiovascular collapse, defined as systolic blood pressure less than 65 mm Hg recorded at least once or less than 90 mm Hg lasting 30 minutes despite 500-1,000 ml of fluid loading (crystalloids solutions) or requiring introduction or increasing doses by more than 30% of vasoactive support, cardiac arrest, death during intubation; moderate: difficult intubation, severe ventricular or supraventricular arrhythmia requiring intervention, oesophageal intubation, agitation, pulmonary aspiration, dental injuries
Time Frame
1 hour after intubation
Other Pre-specified Outcome Measures:
Title
Lowest SpO2 up to 24 hours after intubation
Description
Assessment of the value of the lowest SpO2
Time Frame
up to 24 hours after intubation
Title
Highest positive end expiratory pressure (PEEP) up to 24 hours after intubation
Description
Assessment of the value of the highest PEEP
Time Frame
up to 24 hours after intubation
Title
Highest fraction of inspired oxygen (FiO2) up to 24 hours after intubation
Description
Assessment of the value of the highest FiO2
Time Frame
up to 24 hours after intubation
Title
lowest SpO2 < 90%
Description
incidence of lowest SpO2 less than 90% from induction to 2 minutes after intubation
Time Frame
during intubation
Title
Change in SpO2
Description
Change in SpO2 from SpO2 at induction to lowest SpO2
Time Frame
during intubation
Title
desaturation
Description
desaturation, defined as a change in SpO2 of more than 3% from induction to 2 minutes after intubation
Time Frame
during intubation
Title
Cormack Lehane
Description
Cormack-Lehane grade of glottic view
Time Frame
during intubation
Title
difficulty of intubation
Description
operator-assessed difficulty of intubation
Time Frame
during intubation
Title
additional airway equipment or second operator
Description
need for additional airway equipment or a second operator
Time Frame
during intubation
Title
laryngoscopy attempts
Description
number of laryngoscopy attempts
Time Frame
during intubation
Title
Lowest SpO2 from 0-1 hour post intubation
Description
Assessment of the value of the lowest SpO2 from 0-1 hours after intubation
Time Frame
up to 1 hour after intubation
Title
Highest FiO2 from 0-1 hour post intubation
Description
Assessment of the value of the highest FiO2 from 0-1 hours after intubation
Time Frame
up to 1 hour after intubation
Title
Highest PEEP from 0-1 hour post intubation
Description
Assessment of the value of the highest PEEP from 0-1 hours after intubation
Time Frame
up to 1 hour after intubation
Title
Lowest SpO2 from 1-6 hours post intubation
Description
Assessment of the value of the lowest SpO2 from 1-6 hours after intubation
Time Frame
From 1 to 6 hours after intubation
Title
Highest FiO2 from 1-6 hours post intubation
Description
Assessment of the value of the highest FiO2 from 1-6 hours after intubation
Time Frame
From 1 to 6 hours after intubation
Title
Highest PEEP from 1-6 hours post intubation
Description
Assessment of the value of the highest PEEP from 1-6 hours after intubation
Time Frame
From 1 to 6 hours after intubation
Title
new infiltrate
Description
new infiltrate on chest imaging in the 48 hours after intubation
Time Frame
Up to 48 hours after intubation
Title
new pneumothorax
Description
new pneumothorax on chest imaging in the 24 hours after intubation
Time Frame
Up to 24 hours after intubation
Title
new pneumomediastinum
Description
new pneumomediastinum on chest imaging in the 24 hours after intubation
Time Frame
Up to 24 hours after intubation
Title
Intensive care unit (ICU) length of stay
Description
ICU length of stay
Time Frame
Up to 90 days after intubation
Title
ICU-free days
Description
ICU-free days
Time Frame
Up to 90 days after intubation
Title
invasive ventilator-free days
Description
invasive ventilator-free days
Time Frame
Up to 90 days after intubation
Title
mortality rate on day 28
Description
mortality rate on day 28
Time Frame
Up to 28 days after intubation
Title
In hospital mortality
Description
in hospital mortality
Time Frame
Up to 90 days after intubation
Title
mortality rate on day 90
Description
mortality rate on day 90
Time Frame
Up to 90 days after intubation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must be present in the intensive care unit (ICU) and require mechanical ventilation through an orotracheal tube. Adult (age ≥ 18 years) Subjects must be covered by public health insurance Written informed consent from the patient or proxy (if present) before inclusion or once possible when patient has been included in a context of emergency. Exclusion Criteria: Refusal of study participation or to pursue the study by the patient Pregnancy or breastfeeding Absence of coverage by the French statutory healthcare insurance system protected person intubation in case of cardio circulatory arrest Previous intubation during the same ICU stay and already included in the study
Facility Information:
Facility Name
Centre Hospitalier Universitaire Montpellier, Saint Eloi
City
Montpellier
State/Province
Languedoc-Roussillon
ZIP/Postal Code
34295
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
12 months after the main publication
IPD Sharing Access Criteria
Data are provided to qualified investigators free of charge. Required documents to request data include a summary of the research plan, request form, and institutional review board (IRB) review. Dataset will be shared after careful examination by the study board of investigators.
Citations:
PubMed Identifier
33033014
Citation
Jaber S, Rolle A, Jung B, Chanques G, Bertet H, Galeazzi D, Chauveton C, Molinari N, De Jong A. Effect of endotracheal tube plus stylet versus endotracheal tube alone on successful first-attempt tracheal intubation among critically ill patients: the multicentre randomised STYLETO study protocol. BMJ Open. 2020 Oct 7;10(10):e036718. doi: 10.1136/bmjopen-2019-036718.
Results Reference
derived

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Effect of Endotracheal Tube Plus STYLET Versus Endotracheal Tube Alone

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