Video-guided Percutaneous Tracheostomy (PCT): A Feasibility Study
1 other identifier
interventional
10
1 country
1
Brief Summary
The purpose of this study is to determine the feasibility, safety and effectiveness of an endotracheal tube embedded with a mini video-camera as a guiding tool for percutaneous tracheostomy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2010
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 11, 2009
CompletedFirst Posted
Study publicly available on registry
November 13, 2009
CompletedStudy Start
First participant enrolled
January 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2010
CompletedNovember 13, 2009
November 1, 2009
5 months
November 11, 2009
November 12, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
procedure-related complications
6h
Secondary Outcomes (1)
operative time
minutes
Study Arms (1)
Video-guided PCT
EXPERIMENTALPatients that will be extubated and re-intubated with the ETT-TVT, and monitored throughout intubation and PCT
Interventions
extubation and then re-intubation with the ETT-TVT, followed by video monitoring of the PCT procedure via the ETT-TVT
Eligibility Criteria
You may qualify if:
- The investigators will enroll for this study
- patients aged \> 18 years old, admitted to the ICU,
- who require elective PCT for prolonged mechanical ventilation, airway protection or weaning failure.
You may not qualify if:
- Patients indicated for surgical tracheostomy, due to altered or difficult local anatomy;
- necessity of emergency airway access due to acute airway compromise;
- evidence of infection in the soft tissues of the neck;
- coagulation abnormalities (INR\>1.5, PTT\>40, thrombocyte count \< 50,000);
- gross distortion of the neck anatomy (due to hematoma/tumor/thyromegaly/scarring from previous neck surgery/ unstable C-spine);
- contra-indication for re-intubation/suspected loss of airway during re-intubation;
- hemodynamic instability.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tel-Aviv Sourasky Medical Center
Tel Aviv, 64239, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Patrick Sorkine, MD
Tel-Aviv Sourasky Medical Center
- STUDY CHAIR
Idit Matot, MD
Tel-Aviv Sourasky Medical Center
- PRINCIPAL INVESTIGATOR
Dima Shmain, MD
Tel-Aviv Sourasky Medical Center
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER GOV
Study Record Dates
First Submitted
November 11, 2009
First Posted
November 13, 2009
Study Start
January 1, 2010
Primary Completion
June 1, 2010
Study Completion
August 1, 2010
Last Updated
November 13, 2009
Record last verified: 2009-11