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Transtracheal InjectionNCT01495273

Electrically Guided Needle Insertion: Transtracheal Injection

A study testing Transtracheal injection in people with Transtracheal Injection and Fibreoptic Intubation, run by University of Alberta at 1 site in Canada.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

Various medical procedures require different objects to be inserted into the airway; for example, a bronchoscope - a fibreoptic camera device - can be guided down the windpipe to gain real-time images of the airway. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Transtracheal injection
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
1 siteCanada
Study dates
May 2017to Jan 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adult (18 years of age or older) patients who have provided informed consent.
  • Require awake fibreoptic intubation.

Who cannot join

  • Inability to consent due to language barrier or incapacity to consent.
  • Known upper airway pathologies
  • Known oro-pharyngeal or laryngeal disease, including any swelling, tumour, or infection.
  • Previous radiotherapy or operations on the neck.
  • Cervical spine fractures.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • University of Alberta Hospital

    Edmonton, Alberta, T6G 2B7

Other trials in Canada

About this study

Official title: Adaptation of Nerve Stimulation Technology to Aid Transtracheal Needle Insertion and Injection

Various medical procedures require different objects to be inserted into the airway; for example, a bronchoscope - a fibreoptic camera device - can be guided down the windpipe to gain real-time images of the airway. Since inserting objects down the throat is uncomfortable for most patients, doctors have several options, one of which is putting the patient to sleep using general anesthetic before inserting something into the windpipe. This may not always be the best option, especially in cases where the patient needs to be awake during the procedure. In these cases, the doctor may 'freeze' the windpipe before inserting a scope or a tube into the airway. For this, the doctor inserts a needle through the front of the neck and injects local anesthetic. Inserting a needle into the windpipe comes with some risks to the patient, and the doctor wants to avoid puncturing nearby structures, such as arteries, veins, and the esophagus. The investigators have come up with a new method for accurately guiding a needle into the airway that will alert the user when they have successfully placed the needle tip in the windpipe. The investigators hypothesize that this new method will prove to be beneficial to clinicians and emergency medical personnel who need a fast, easy, and reliable way to insert a needle into the airway.

Read the detailed description

Background and rationale

The trachea can be anesthetized by several different methods, one of which is transtracheal injection of a local anesthetic such as lidocaine. This technique is performed to prepare a patient for a variety of procedures, including awake fibreoptic intubation and cricothyroidotomy. Tracheal anesthesia is performed by first identifying the cricothyroid ligament; this structure is generally located by placing one finger on the thyroid cartilage and another on the cricoid cartilage. Approximately 4-6 mL of local anesthetic is delivered through a small needle or an intravenous catheter inserted in the neck midline. Anesthesia occurs quickly and permits the patient to be awake and aware during the procedures that follow.

Insertion of a needle into the trachea is not without risk to the patient. Several complicating factors affect the success rate of tracheal needle insertion, and in emergency situations where oxygen must be delivered through the insertion site, as in cricothyroidotomy, accurate needle insertion can mean the difference between life and death for the patient. One complicating factor in this procedure is that the thyroid cartilage and the cricoid cartilage can be difficult to identify, especially in obese people. Needle insertion is made more complicated due to the anatomy surrounding the cricothyroid membrane: the carotid artery and jugular vein lie laterally to the membrane, the cricothyroid artery is located superiorly and laterally, and the highly vascularized thyroid gland is located inferiorly. Intravascular injection of anesthetic can lead to a seizure, and inaccurate injection could lead to anesthesia of surrounding nerves. There is also a risk of puncturing through the posterior wall of the trachea, which may cause esophageal perforation.

Given these complications, a quick and easy method of ensuring accurate tracheal needle insertion, while avoiding damage to surrounding tissues, would greatly benefit clinicians and could potentially save lives in emergency situations. We wish to evaluate a simple technique to guide a needle tip into the trachea that mitigates the risks of conventional methods of needle insertion. We will use nerve stimulation equipment to aid in the guidance and placement of a needle tip into the tracheal lumen, which we predict will be faster and more accurate than current conventional methods. The nerve stimulation technology can alert the user to the exact moment the needle tip is suspended in the trachea and also alerts the user to when the needle tip is in contact with body tissue, avoiding accidental puncture of the lateral and posterior tracheal walls. We believe that this method of electrically-guided needle insertion will be a significant improvement over current methods of percutaneous needle insertion and transtracheal injection.

Study objective To assess the value of nerve stimulation equipment for guidance and placement of a needle-catheter assembly for transtracheal injection.

Hypothesis Nerve stimulation equipment will help the physician guide and insert the needle tip into the tracheal lumen with more accuracy than conventional techniques.

Study Design This is a prospective, descriptive, interventional study.

Study Procedures This study will involve recruiting consenting patients undergoing procedures that require awake fibreoptic intubation following transtracheal injection of local anesthetic. We intend to recruit 30 patients, who will be randomized into two groups, one (experimental) that will undergo transtracheal injection using a needle connected to a nerve stimulation device, and another (control) that will receive tracheal anesthetic using standard, conventional needle insertion and injection technique.

Patients will lay supine with the head and neck in a neutral position on one pillow. The physician will locate the cricothyroid ligament, through which the needle-catheter assembly will be inserted. In the experimental group, a 21G 64 mm insulated needle with an 18G catheter assembly (MultiSet, Pajunk, Germany) and a commonly used nerve stimulator (HNS 12, B.Braun, Germany) will be used to access the airway (this nerve stimulator device has been approved for use on live patients in Canada and is a common piece of equipment in operating rooms). The nerve stimulator will be connected to a current meter, and a ground electrode will be attached to the body. When the needle tip is in contact with body tissue (i.e., tracheal wall), the electrical circuit will be closed, producing a reading of 1.0 mA on the current reader. Suspension of the needle tip in the airway will interrupt the circuit, producing a reading of 0.0 mA. In addition, an audible signal built into the nerve stimulator will alert the user to a change in current, warning that the needle tip has advanced too far and is in contact with the posterior or lateral tracheal wall. Once the physician has successfully inserted the needle tip into the tracheal lumen, the needle will be withdrawn and 4-6 mL lidocaine (2-4%) will be delivered through the catheter, anesthetizing the airway. Once the airway is anesthetized, a bronchoscope can be guided down the trachea. The control group will undergo an identical procedure, except that no nerve stimulator will be connected to the needle.

For each patient, the physician performing the transtracheal injection will document their opinion of each needle insertion and injection, but no personal information about the patient will be recorded at this time. For both the experimental and control groups, study investigators will collect data documenting the time needed for each needle insertion and the success of each attempt. These data will be statistically analyzed to determine the value of the nerve stimulator-guided technique over the conventional technique.

Being tested
Transtracheal injection

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Transtracheal injectionProcedure or surgery

    Experimental group will undergo transtracheal injection using needle connected to a nerve stimulator device.

  • Transtracheal injectionProcedure or surgery

    Control group will undergo transtracheal injection with a standard needle/syringe assembly.

Study groups in NCT01495273
Study groupRoleWhat they receive
Nerve stimulatorExperimentalExperimental group; will undergo transtracheal injection with needle connected to nerve stimulator.
Receives: Procedure: Transtracheal injection
Standard needle/syringeActive comparatorControl group; will undergo transtracheal injection with standard needle/syringe assembly.
Receives: Procedure: Transtracheal injection

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Needle tip placement in tracheal lumen

    After injection of local anesthetic into the skin of the neck, a needle connected to a syringe containing 4-6 mL 2-4% lidocaine will be inserted through the cricothyroid membrane into the tracheal lumen. Success will be recorded as accurate puncture of the cricothyroid membrane and trachea and injection of lidocaine into the tracheal lumen.

    Measured: From positioning of the patient to anesthesia of the trachea; approximately 10 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Dec 2011 (estimated)
  2. Study startMay 2017 (estimated)
  3. Primary completionDec 2017 (estimated)
  4. Study completionJan 2018 (estimated)

Why it stopped: Study never started, no subjects enrolled

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01495273
Sponsor's protocol ID
Pro00026789
Status last verified
Mar 2020
First submitted
17 Nov 2011
Last updated
24 Mar 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Transtracheal injection in people with Transtracheal Injection and Fibreoptic Intubation, run by University of Alberta at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 24 Mar 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Needle tip placement in tracheal lumen (time frame: From positioning of the patient to anesthesia of the trachea; approximately 10 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Mar 2020.

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