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Catheterization, Central VenousNCT06958731

In-plane Versus Real Time Bi-plane Single-operator Laser-assisted With a Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization:A Randomized Controlled Trial

A study testing TuoRen Ultrasonic System and Huasheng Color Ultrasonic Diagnostic System in people with Catheterization, Central Venous and Ultrasound Guided, run by The First Hospital of Jilin University at 1 site in China.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Background: Ultrasound guidance is an important technique to improve the success rate of internal jugular vein catheterization (IJVC) at the first-attempt, however, both long-axis in-plane and short-axis out-of-plane techniques have their own disadvantages. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
TuoRen Ultrasonic System and Huasheng Color Ultrasonic Diagnostic System
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
352 participants
Where
1 siteChina
Study dates
12 Jan 2026to 1 Jun 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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

  • The patient fully understood the benefits and risks of the study, voluntarily participated, and signed the informed consent form
  • Require internal jugular vein catheterization
  • ASA grade I~IV
  • Over 18 years and older

Who cannot join

  • Congenital malformation or abnormal development of the internal jugular vein;
  • Prior internal jugular vein catheterization performed within the past month
  • Puncture site injury, infection, or hematoma
  • History of surgical intervention in the right neck region
  • Restricted neck mobility due to prior surgery or traumatic injury

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site
  • the first hospital of Jilin University

    Changchun, Jilin, 130021

Other trials in China

About this study

Official title: In-plane Versus Real-time Bi-plane Single-operator Laser-assisted With an Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization: A Randomized Clinical Trial

Background: Ultrasound guidance is an important technique to improve the success rate of internal jugular vein catheterization (IJVC) at the first-attempt, however, both long-axis in-plane and short-axis out-of-plane techniques have their own disadvantages. The T-shaped ultrasonic probe invented by us combined with the help of laser positioning and 3D printing manipulator could realize real-time bi-plane guidance of the needle short-axis out-of-plane and long-axis in-plane. With the help of the Single-operator Laser-assisted T-shaped probe, the whole process of needle insertion, guide wire placement and catheter placement can be visualized, which is expected to improve the success rate on the first-attempt.

Objective: The primary outcome was the first-attempt success rate of initial RIJV catheterization without complications. The completion of the catheterization was defined as the presentation of the CVP waveform on the monitor. The secondary outcomes included first-attempt puncture success rate,first-attempt catheterisation success rate,overall catheterisation success rate,first-attempt needle tip location,first-attempt needle tip midline placement rate,number of needle direction adjustments,number of ultrasound probe repositionings, number of puncture attempts,first-attempt localisation time,first-attempt guidewire insertion success time,overall catheterisation success time.

Read more

Design, Setting, and Participants: This single-center, prospective, parallel-group, randomized controlled study enrolled surgical patients over 18 years and older (ASA grade Ⅰ-Ⅳ) who required IJVC ,fully understands the benefits and risks of the study, participates voluntarily, and signs the informed consent form in the First Hospital of Jilin University. The exclusion criteria were congenital abnormal development of the internal jugular vein; prior puncture at the same site last month; puncture site injury, infection, or hematoma; right neck surgery history and neck fixation due to surgery or injury. The participants were randomized into the traditional ultrasound-guidance group or the single-operator Laser-assisted T-shaped probe ultrasound-guidance group. After inducing general anesthesia, ultrasound-guided internal jugular vein catheterization was performed by the experienced operators.

Interventions: 352 patients were stratified into eight subgroups based on whether common carotid artery coverage exceeded 50% ,internal jugular vein depth exceeded 10mm , and internal jugular vein anteroposterior diameter exceeded 10mm . Each subgroup generated an independent randomisation sequence according to the block randomisation principle (T-mode ultrasound-guided group and 'long-axis plane' ultrasound-guided group). Upon enrolment, new subjects were assigned to corresponding subgroups based on stratification factors. Within each subgroup's dedicated random sequence, the allocation plan (T-shaped ultrasound guidance group or 'long-axis plane' ultrasound guidance group) was sequentially retrieved and marked. The next subject in that subgroup would receive the subsequent plan in the sequence. The operating team comprised six physicians (including two residents, two specialists, and two anaesthesiologists), who were not involved in other aspects of the study. Given the significant technical differences between the two approaches, the operators, equipment assistants, and research assistants were aware of the groupings. Conversely, participants' families were unaware of the groupings and could withdraw from the trial at any time. All data were collected and analysed by the same research assistant.

Read the detailed description

After the patient was admitted to the operating room, the vital signs of the patients were monitored,the thoraco-chin distance (the distance between the mandible and the upper edge of the sternostemma in cm when the patient's head was tilted back as far as possible) and neck circumference (the thinest neck, that is, the upper edge of the 7th cervical vertebra to the horizontal position below the Adam's apple in cm) were measured and recorded in the supine position. After the establishment of peripheral venous access, the patients received rapid induction of general anesthesia and tracheal intubation. Without special circumstances, the right internal jugular vein was selected by the operator after randomization. The probe frequency of 13 MHz and a depth of 4.0 cm were set for optimal image quality in both groups. The patient was placed in a supine position with the head 15 degrees lower and the head turned to the left to fully expose the right side of the neck, and a thin pillow was placed under the right shoulder if necessary.

T-type ultrasound guidance unit:

A 3D marking laser with laser emitter is mounted on the T-type ultrasound probe.The laser emitter is positioned directly above the Mark point on the short-axis plane of the T-shaped ultrasound probe. Due to the probe's hardware structure-where the long and short-axis probes are vertically and tightly fused, with the long-axis probe's centreline perpendicular to and passing through the short-axis probe's centreline-the emitted laser lies on the skin surface extension of the short-axis plane's centreline. Instruct the assistant to apply an appropriate amount ofcoupling agent evenly onto the ultrasound probe. The operator and assistant collaborate to cover the entire 3D-printed three-axis adjustable support arm and ultrasound probe with a sterile sleeve, evacuating any air between the probe and the sleeve. Coupling agent is then applied evenly to the outer layer of the sterile sleeve where it contacts the patient's skin,completing the equipment preparation. To commence positioning, the operator controls gently place the T-shaped ultrasound probe onto the patient's neck skin, positioning the short axis cephalad and the long axis caudally.Adjust the arm and rotation axis so the midline of the short-axis image centres the transverse section of the internal jugular vein. The laser direction now indicates the cutaneous pathway to the vein's centre point, coinciding with the long-axis probe's midline. Adjust the slide rail to align the midpoint of the short-axis probe with the marked point, then continue sliding 1 cm cephalad to ensure the needle tip approaches the maximum transverse plane level upon subcutaneous entry into the internal jugular vein. Positioning is complete. Secure the arm to stabilise the probe against the skin surface, establishing hands-free, stable, and continuously monitored ultrasound guidance. The operator's left hand stabilises the skin near the puncture site.

The right hand holds the puncture needle at a 45° angle to the skin, with the needle body aligned with the laser path and closely following the short-axis probe's MARK point during insertion, while simultaneously performing aspiration. Once the needle tip enters the subcutaneous tissue, if deviation is observed in the short-axis ultrasound image, adjust the insertion angle to penetrate the anterior wall directly above the internal jugular vein. Upon visualising needle entry into the vessel on both short-axis and long-axis ultrasound images, and observing uninterrupted, non-pulsatile venous blood return in the syringe, adjust the needle tip position to the centre of the longitudinal section of the internal jugular vein using the long-axis view. Subsequently, while maintaining the needle position with the left hand, slide the probe distally with the right hand and determine the needle tip position prior to guidewire placement using the 'dynamic needle tip method' via the short-axis plane image. Save a screenshot for the initial needle tip position assessment. During this attempt, the needle tip position remains fixed. Insert the guidewire 30 cm without resistance through the lumen at the rear end of the syringe connected to the tip of the puncture needle. Under guidewire guidance, place the guide catheter 12-15 cm into the internal jugular vein. If resistance persists, withdraw the guidewire and puncture needle from the internal jugular vein and apply pressure to the puncture site with sterile gauze for approximately 3 minutes. Subsequent attempts may proceed once no significant bleeding is observed at the puncture site. During this process, the timer shall not be paused, and the number of ultrasound probe repositionings and needle tip adjustments shall be recorded throughout.

Ultrasound-guided group within the longitudinal axis plane:

The assistant applies coupling agent to the surface of the ultrasound probe. The operator and assistant collaborate to cover the probe with a sterile sleeve, evacuating any air between the probe and sleeve. Coupling agent is then evenly applied to the outer layer of the sterile sleeve where it contacts the patient's skin, completing device preparation. To commence localisation, the operator holds the ultrasound probe with the left hand, aligning its longitudinal axis parallel to the course of the internal jugular vein. After superimposing the midpoint of the probe's longitudinal axis plane with the marked point, the probe is slid further along the longitudinal axis towards the cephalic direction by 1 cm. This ensures the needle tip approaches the most transverse plane. Stabilise the probe with the left hand to complete positioning.Hold the puncture needle at a 45° angle to the skin with the needle body aligned along the longitudinal axis.

Advance the needle closely alongside the midpoint of the probe's longitudinal axis while aspirating.Upon subcutaneous entry, if the needle trajectory deviates on the longitudinal ultrasound image, adjust the insertion angle or reposition the probe to ensure the needle tip penetrates directly above the internal jugular vein.

After confirming vascular entry on ultrasound and observing unobstructed venous blood return in the syringe, adjust the needle tip position to ensure the needle tip penetrates directly above the internal jugular vein. Upon visualising vascular entry in the ultrasound image and observing uninterrupted, pulsatile venous blood in the syringe, adjust the needle tip position to align it with the midpoint of the longitudinal axis plane of the internal jugular vein. At this stage, the right hand should stabilise the needle immovably, while the left hand manipulates the ultrasound probe to determine the needle tip position relative to the longitudinal axis plane using the the 'dynamic needle tip method' to determine the needle tip position prior to guidewire placement. Save a screenshot for the initial needle tip position assessment. During this attempt, the needle tip position remains unchanged. Insert the guidewire 30 cm without resistance through the lumen at the end of the syringe connected to the needle tip. Under guidewire guidance, place a 12-15 cm internal jugular vein catheter and secure it properly. Should significant resistance occur during guidewire insertion, withdraw the wire. After repositioning the ultrasound probe and adjusting the intravascular needle tip, reinsert the guidewire.If resistance persists, withdraw both the guidewire and puncture needle from the internal jugular vein. Apply pressure to the puncture site with sterile gauze for approximately 3 minutes.

The operation timer shall not be paused during this interval, and the number of ultrasound probe repositionings and needle tip adjustments shall be recorded throughout.

From patient admission to the operating theatre until completion of follow-up, the research assistant shall tick and record the following data in the CRF form: age, gender, height, weight, surgical scheduling (elective or emergency), surgical category, ASA classification, comorbidities, pre-procedural MAP, presence of coagulation, anticoagulant therapy status, antiplatelet therapy status,sternocleidomastoid distance, neck circumference, anterior/posterior jugular vein diameter and depth, common carotid artery coverage, initial catheterisation success, initial puncture success, initial needle tip position score, needle tip adjustment count, ultrasound probe repositioning count, total attempts, device preparation time, initial positioning time, initial guidewire Overall catheterisation success time, occurrence of complications (posterior jugular vein puncture, arterial puncture, haematoma, haemothorax, pneumothorax, nerve injury, jugular vein thrombosis), operator's assessment of the procedure (0-10 points, 0 being dissatisfied, 10 being highly satisfied).

Being tested
TuoRen Ultrasonic System, Huasheng Color Ultrasonic Diagnostic System
Keywords
internal jugular vein catheterization, ultrasound guided

What participants receive

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

  • TuoRen Ultrasonic SystemDevice

    The Single-operator Laser-assisted T-shaped probe consisted of TuoRen Ultrasonic System (TUR200, Shenzhen Tuoren Bio-Medical Electronics Co., LTD) with a T-shaped probe (L38T7C), a 3D-printed probe-carrying enclosure with a linear laser transmitter ( ZLM120AL650-22130BXS, Shenzhen Zhonglai Technology Co., Ltd.) and ultrasonic probe manipulator.

  • Huasheng Color Ultrasonic Diagnostic SystemDevice

    Ultrasonic (Huasheng Color Ultrasonic Diagnostic System, Navi s, Shenzhen Huasheng Medical Technology Co., LTD.) and a 4.0MHz phased probe were used for the long-axis in-plane internal jugular vein catheterization

Study groups in NCT06958731
Study groupRoleWhat they receive
the single-operator Laser-assisted T-shaped probe ultrasound-guidance groupExperimentalNot described
Receives: Device: TuoRen Ultrasonic System
traditional ultrasound-guided in-plane groupExperimentalNot described
Receives: Device: Huasheng Color Ultrasonic Diagnostic System

What is being measured

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

  1. the first-attempt success rate of internal jugular vein catheterization without complications

    Measured: perioperative/periprocedural

Secondary outcomes (12)
  1. First-attempt puncture success rate

    Measured: perioperative/periprocedural

  2. Overall catheterization success rate

    Measured: perioperative/periprocedural

  3. First-attempt needle tip positioning score

    Divide the cross-section of the internal jugular vein into 12 quadrants, assigning each quadrant a score based on its position within the quadrant, ranging from a minimum of 1 point to a maximum of 5 points.The Higher the score,the closer it is to the midpoint of the cross-section.

    Measured: perioperative/periprocedural

  4. Midpoint accuracy rate of needle tip placement on first attempt

    Measured: perioperative/periprocedural

  5. Number of needle direction adjustments during puncture

    Measured: perioperative/periprocedural

  6. Number of ultrasound probe repositionings

    Measured: perioperative/periprocedural

  7. Total number of puncture attempts

    Measured: perioperative/periprocedural

  8. Time to initial target localization

    Measured: perioperative/periprocedural

  9. Successful guidewire insertion time on first attempt

    Measured: perioperative/periprocedural

  10. Total successful catheterization duration

    Measured: perioperative/periprocedural

  11. Complication incidence rate

    Measured: perioperative/periprocedural

  12. Operator satisfaction score

    Measured: perioperative/periprocedural

Timeline

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

  1. First posted6 May 2025
  2. Study start12 Jan 2026
  3. Primary completion21 May 2026
  4. Study completion1 Jun 2026 (estimated)

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
352 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06958731
Sponsor's protocol ID
2025-169
Status last verified
Jan 2026
First submitted
20 Apr 2025
Last updated
28 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing TuoRen Ultrasonic System and Huasheng Color Ultrasonic Diagnostic System in people with Catheterization, Central Venous and Ultrasound Guided, run by The First Hospital of Jilin University at 1 site in China.

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 4 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: enrolling by invitation, as of the sponsor's last update on 28 May 2026. 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 China. 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?

This study is still under way. Results are not available in the source record yet.

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?

the first-attempt success rate of internal jugular vein catheterization without complications (time frame: perioperative/periprocedural). 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 28 May 2026.

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