Conventional Intubation Versus VivaSight™-SL (VivaITN)
Primary Purpose
Respiratory Insufficiency
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
VivaSight intubation
conventional intubation
Sponsored by
About this trial
This is an interventional treatment trial for Respiratory Insufficiency focused on measuring intubation, intratracheal, critical care
Eligibility Criteria
Inclusion Criteria:
- Patients receiving urgent or elective endotracheal intubation in the Dept. of Intensive Care Medicine.
- Age ≥ 18 years
- Informed consent
Exclusion Criteria:
- Age < 18 years
- No consent
Sites / Locations
- Universitätsklinikum Hamburg-Eppendorf
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
VivaSight intubation
conventional intubation
Arm Description
Patients are intubated with the VivaSight-SL endotracheal tube
Patients are intubated with a conventional endotracheal tube
Outcomes
Primary Outcome Measures
first attempt success rate
after first attempt of intubation
total number of attempts to successful intubation
after successful intubation
Secondary Outcome Measures
average number of attempts for intubation
after successful intubation
time to successful intubation
after successful intubation
time to successful intubation with one attempt
after first attempt successful intubation, if applicable
vomiting or aspiration during intubation
after successful intubation
accidental esophageal intubation
after successful intubation
decrease of SpO2 < 80%
after successful intubation, SpO2: oxygen saturation by pulse oximetry
hypotension
after successful intubation, hypotension defined as systolic blood pressure < 70mmHg
Full Information
NCT ID
NCT02837055
First Posted
June 13, 2016
Last Updated
January 19, 2018
Sponsor
Universitätsklinikum Hamburg-Eppendorf
1. Study Identification
Unique Protocol Identification Number
NCT02837055
Brief Title
Conventional Intubation Versus VivaSight™-SL
Acronym
VivaITN
Official Title
Prospective, Randomized Study in Critically Ill Patients Receiving Endotracheal Intubation: Comparison Between a Conventional Approach and Video Assisted Intubation by the VivaSight™-SL Tube
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
April 2016 (undefined)
Primary Completion Date
January 12, 2018 (Actual)
Study Completion Date
January 12, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
It has been shown that videolaryngoscopy may be superior to direct laryngoscopy for endotracheal intubation in intensive care. Recently, an endotracheal tube with an integrated camera at its tip has been introduced (VivaSight-SL) allowing for direct visual confirmation of the tube's passage through the vocal cords during intubation.
Patients who are requiring urgent or endotracheal intubation in intensive care are randomized to receive either a conventional intubation with direct laryngoscopy or to receive intubation with the VivaSight-SL-Tube. Primary outcome measures are first attempt success rate and number of attempts to successful intubation.
Detailed Description
Background
Airway management in critically ill patients is usually performed by endotracheal intubation with direct laryngoscopy. [1, 2] However, it has been shown that videolaryngoscopy may be superior to the conventional approach in intensive care, i. e. the number of attempts to successful intubation and the rate of accidental esophageal intubation are lower and the visualization of the vocal chords is improved. [3, 4]
Recently, an endotracheal tube with an integrated camera at its tip has been introduced that permits a continuous visualization of the tube's insertion into the trachea on a monitor connected to the camera (VivaSightTM-SL, ETView Ltd., Misgav, Israel) [5]. This tube has been CE and FDA certified (http://www.etview.com/products/vivasight-sl).
It is possible to observe the passage of the tube through the vocal chords during intubation and to verify the correct placement by visualization of the tracheal cartilage. This is an advantage over videolaryngoscopy, in which the camera is mounted on the laryngoscope blade. For the VivaSightTM-SL tube, a decrease for time to intubation and an increase of first attempt success has been shown over conventional intubation in a simulator trial. [6]
In this study, the VivaSightTM-SL tube is tested against the conventional approach during elective and urgent intubations in critically ill patients.
Methods
Study design: randomized, prospective trial
Sample size: n = 54
With a sample size of 54 (randomized 1:1 as 2x 27) a difference of 35% for first attempt success over conventional intubation may be detected with an α-error of 0,05 and a β-error of 1-0,8.
Duration of study: until sample size reached or 18 months after begin of study
Procedures:
screening of patients for study inclusion according to inclusion and exclusion criteria
conventional endotracheal intubation by direct laryngoscopy
endotracheal intubation with the VivaSightTM-SL tube
study inclusion:
All patients being treated in the Dept. of Intensive Care Medicine receiving percutaneous tracheotomy due to long term ventilation are screened according to inclusion and exclusion criteria.
Details of study related procedures:
Intubation:
The Intubation with the VivaSightTM-SL endotracheal tube does not differ from an intubation with a conventional tube that is done with respect to the standard operating procedure (SOP) of the Dept. of Intensive Care Medicine. Additionally, the intubation is guided by the camera mounted on the tip of the tube. During the intubation, vital parameters are monitored with respect to the underlying disease and patients' therapy is continuously adjusted. According to the SOP, two physicians are present of which at least one is a fellow or an attending physician with experience in intensive care medicine. In this trial, intubation is done exclusively by a fellow or attending physician.
Consent: all patients or their legal surrogate give written informed consent.
Data protection: Data are anonymized.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Insufficiency
Keywords
intubation, intratracheal, critical care
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
54 (Actual)
8. Arms, Groups, and Interventions
Arm Title
VivaSight intubation
Arm Type
Experimental
Arm Description
Patients are intubated with the VivaSight-SL endotracheal tube
Arm Title
conventional intubation
Arm Type
Active Comparator
Arm Description
Patients are intubated with a conventional endotracheal tube
Intervention Type
Device
Intervention Name(s)
VivaSight intubation
Intervention Description
patients are intubated with an endotracheal tube with an integrated camera
Intervention Type
Device
Intervention Name(s)
conventional intubation
Intervention Description
patients are intubated with a conventional endotracheal tube
Primary Outcome Measure Information:
Title
first attempt success rate
Description
after first attempt of intubation
Time Frame
day 1
Title
total number of attempts to successful intubation
Description
after successful intubation
Time Frame
day 1
Secondary Outcome Measure Information:
Title
average number of attempts for intubation
Description
after successful intubation
Time Frame
day 1
Title
time to successful intubation
Description
after successful intubation
Time Frame
day 1
Title
time to successful intubation with one attempt
Description
after first attempt successful intubation, if applicable
Time Frame
day 1
Title
vomiting or aspiration during intubation
Description
after successful intubation
Time Frame
day 1
Title
accidental esophageal intubation
Description
after successful intubation
Time Frame
day 1
Title
decrease of SpO2 < 80%
Description
after successful intubation, SpO2: oxygen saturation by pulse oximetry
Time Frame
day 1
Title
hypotension
Description
after successful intubation, hypotension defined as systolic blood pressure < 70mmHg
Time Frame
day 1
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients receiving urgent or elective endotracheal intubation in the Dept. of Intensive Care Medicine.
Age ≥ 18 years
Informed consent
Exclusion Criteria:
Age < 18 years
No consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefan Kluge, MD, PhD
Organizational Affiliation
Head of Dept. of Intensive Care Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitätsklinikum Hamburg-Eppendorf
City
Hamburg
State/Province
HH
ZIP/Postal Code
20246
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
25254395
Citation
Braune S, Kluge S. [Airway management]. Dtsch Med Wochenschr. 2014 Oct;139(40):2003-5. doi: 10.1055/s-0034-1387247. Epub 2014 Sep 25. No abstract available. German.
Results Reference
background
PubMed Identifier
20077384
Citation
Pothmann W, Kluge S. [Endotracheal intubation]. Dtsch Med Wochenschr. 2010 May;135(3):94-7. doi: 10.1055/s-0029-1244824. Epub 2010 Jan 14. No abstract available. German.
Results Reference
background
PubMed Identifier
24125064
Citation
Mosier JM, Whitmore SP, Bloom JW, Snyder LS, Graham LA, Carr GE, Sakles JC. Video laryngoscopy improves intubation success and reduces esophageal intubations compared to direct laryngoscopy in the medical intensive care unit. Crit Care. 2013 Oct 14;17(5):R237. doi: 10.1186/cc13061.
Results Reference
background
PubMed Identifier
25479112
Citation
Silverberg MJ, Li N, Acquah SO, Kory PD. Comparison of video laryngoscopy versus direct laryngoscopy during urgent endotracheal intubation: a randomized controlled trial. Crit Care Med. 2015 Mar;43(3):636-41. doi: 10.1097/CCM.0000000000000751.
Results Reference
background
PubMed Identifier
23121322
Citation
Huitink JM, Koopman EM, Bouwman RA, Craenen A, Verwoert M, Krage R, Visser IE, Erwteman M, van Groeningen D, Tijink R, Schauer A. Tracheal intubation with a camera embedded in the tube tip (Vivasight() ). Anaesthesia. 2013 Jan;68(1):74-8. doi: 10.1111/anae.12065. Epub 2012 Nov 5.
Results Reference
background
PubMed Identifier
26020389
Citation
Kurowski A, Szarpak L, Truszewski Z, Czyzewski L. Can the ETView VivaSight SL Rival Conventional Intubation Using the Macintosh Laryngoscope During Adult Resuscitation by Novice Physicians?: A Randomized Crossover Manikin Study. Medicine (Baltimore). 2015 May;94(21):e850. doi: 10.1097/MD.0000000000000850. Erratum In: Medicine (Baltimore). 2015 Jun;94(25):1.
Results Reference
background
PubMed Identifier
30241488
Citation
Grensemann J, Eichler L, Wang N, Jarczak D, Simon M, Kluge S. Endotracheal tube-mounted camera-assisted intubation versus conventional intubation in intensive care: a prospective, randomised trial (VivaITN). Crit Care. 2018 Sep 22;22(1):235. doi: 10.1186/s13054-018-2152-4.
Results Reference
derived
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Conventional Intubation Versus VivaSight™-SL
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