- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01073722
EZ Blocker Versus Left Sided Double-lumen Tube
April 29, 2011 updated by: Radboud University Medical Center
Endobronchial EZ Blocker Compared to Left Sided Double-lumen Tube for One-lung Ventilation
Lung isolation is used to achieve one lung ventilation to facilitate thoracic surgery.
Two methods are commonly used, a double lumen tube (DLT) or a bronchial blocker introduced through a single lumen tube.
However, both techniques have advantages and disadvantages.
Briefly, the DLT can be positioned faster and remains firmly in place, but is sometimes difficult or even impossible to introduce.
The DLT is larger than a conventional single lumen tube and the incidence of postoperative hoarseness and airway injuries is higher.
Compared to the DLT, bronchial blocking devices are more difficult to position and need more frequent intraoperative repositioning.
These disadvantages of the existing devices for lung isolation prompted further development of the bronchial blocker concept.
The design of a new Y shaped bronchial blocker, the EZ- Blocker® (AnaesthetIQ BV, Rotterdam, The Netherlands) (EZB), combines the advantages of both lung isolation techniques.
The aim of the study is to compare in a randomised, prospective way the ease of placement, the incidence of malpositioning and the quality of lung deflation of a left DLT and a EZB.
Secondly, the incidence and severity of damage to laryngeal, tracheal and bronchial structures caused by the use of the DLT or the EZB is a target of the study.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Anticipated)
100
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Gelderland
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Nijmegen, Gelderland, Netherlands, 6500HB
- Department of Anesthesiology, Pain and Palliative Medicine of the Radboud University Nijmegen Medical Centre
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- ASA physical status 1-3 patients
- Patients scheduled for surgery requiring a left sided DLT for single lung ventilation
Exclusion Criteria:
- Contraindications are lesions along the path of the left sided double lumen tube or the EZB
- Tracheal or mainstem bronchial stenosis
- Distorted carinal anatomy,
- Anticipated difficult intubation (Mallampatti score ≥ 3)
- History or presence of tracheostoma
- Patients who require absolute lung separation
- Patients who require sleeve resection of mainstem bronchus
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Left double lumen tube
Traditionally, single lung ventilation is obtained with a double lumen tube (DLT).
In our institution a polyvinyl DLT (Broncho-cath, Mallinckrodt,) without carinal hook, is used.
This type of tube exists of a tube with two lumen with two distal cuffs.
One lumen (called the bronchial lumen) extends some distance further, has a slight curvature and has a small blue cuff.
The other lumen (called the tracheal lumen) has a larger cuff.
A DLT tube exists in four sizes and one can choose in a left or a right configuration.
Almost always, we use a left sided DLT.
A DLT has a much larger diameter than a standard single lumen endotracheal tube
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The gold standard for lung isolation is the use of a double lumen tube (DLT).
A DLT is a bifurcated tube with a bronchial and a tracheal lumen.
Other Names:
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Active Comparator: EZ-blocker
The EZ-blocker (EZB) is a semi-rigid catheter but it has two distal extensions, both with an inflatable cuff and a central lumen.
It is intended for use in combination with a standard single lumen tube.
After the EZB is advanced trough the distal end of the single lumen tube, both extensions spread out and find their way in the left and right main stem bronchi.
The place where the two extensions are attached to the shaft now rests on the carina.
Fiber optic bronchoscopy should be used for proper positioning.
After placement of the EZB, one of the cuffs can be inflated to obtain lung separation under direct visual inspection with fiber optic bronchoscopy.
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Bronchial blockers are balloon-tipped semi-rigid catheters.
Different types are available.
They are not easy to put in position and frequently dislocates during repositioning of the patient or during surgical manipulation.
To solve these problems, a novel type of bronchus blocker, i.e. the EZ- Blocker® is developed.
The EZB is also a semi-rigid catheter but it has two distal extensions, both with an inflatable cuff and a central lumen.
These improvements owe to the fact that the blocker anchors itself on the carina with the two extensions.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
the incidence of malposition of a left sided DLT or the EZB
Time Frame: there are four time points (after insertion of the device, after inflation of cuff or balloon, after repositioning patient, during surgery) were malposition are considered. Total time spend is 3 hours on the day of the operation
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there are four time points (after insertion of the device, after inflation of cuff or balloon, after repositioning patient, during surgery) were malposition are considered. Total time spend is 3 hours on the day of the operation
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
description of damage to laryngeal, tracheal and bronchial structures
Time Frame: videobronchoscopy before and after intervention. Time frame 5 min for each video and additional 5 min for assessment afterwards on the day of the operation
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videobronchoscopy before and after intervention. Time frame 5 min for each video and additional 5 min for assessment afterwards on the day of the operation
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the ease of insertion
Time Frame: the ease of insertion of the devices is qualitative variable: 1= excellent, 2= good, 3=average, 4=poor. Time frame is 5 min on the day of the operation.
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the ease of insertion of the devices is qualitative variable: 1= excellent, 2= good, 3=average, 4=poor. Time frame is 5 min on the day of the operation.
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the incidence of postoperative complains of sore throat and hoarseness
Time Frame: questionnaire (2 questions, time frame is 1 min) after surgery and one day after surgery
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questionnaire (2 questions, time frame is 1 min) after surgery and one day after surgery
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jo Mourisse, Dr., Department of anesthesiology, pain and palliative medicine of the Radboud University Nijmegen Medial Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2010
Primary Completion (Actual)
April 1, 2011
Study Completion (Actual)
April 1, 2011
Study Registration Dates
First Submitted
February 17, 2010
First Submitted That Met QC Criteria
February 22, 2010
First Posted (Estimate)
February 23, 2010
Study Record Updates
Last Update Posted (Estimate)
May 2, 2011
Last Update Submitted That Met QC Criteria
April 29, 2011
Last Verified
August 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- NL30799,091,09
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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