A Percutaneous Ultrasound Device With Needle Guide for Vascular Access

Vascular Access Clinical Trial

Official title:

A Percutaneous Ultrasound Device With Needle Guide for Vascular Access

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03879161
• Other study ID #: IRB00103043
• Secondary ID: R42HL093879R44HL
• Status: Not yet recruiting
• Phase: N/A
• Start date: September 2024
• Est. completion date: December 2026

Study information

• Verified date: January 2024
• Source: Johns Hopkins University
• Contact: Robert Liddell, MD
• Phone: 410-614-5183
• Email: rliddel1[@]jhmi.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This first-in-human pilot study seeks to evaluate the feasibility and safety of using a percutaneous ultrasound device with needle guide for vascular access. Eligible participants will undergo the procedure of transcatheter arterial chemoembolization for primary or metastatic liver cancer, as part of participants' clinical care. The percutaneous ultrasound device with needle guide will be deployed in eligible participants at the beginning of the procedure for guiding a needle inside the femoral artery. Once the needle is inside the artery, then a guide wire is advanced inside the needle and vascular access is successfully obtained.

The study will identify whether this ultrasound-based device with needle guide is helpful for guiding a needle inside the femoral artery.

Description:

This NIH Small Business Innovation Research (SBIR)-funded study seeks to test a forward-viewing, ultrasound (US)-based device with needle guide for vascular access.

Access to large arteries is an indispensable step of any trans-arterial catheterization procedure. Surface US-guided vascular cannulation greatly improves first-pass success and reduces complications and is recommended as the preferred technique by numerous specialties and governmental agencies. Surface US-guided cannulation has several key limitations, including dependence on operator skills and experience. Safety and success of vascular access could be vastly improved with a single integrated imaging/interventional device with a small footprint that enables a single-hand operation of the US probe and visualizes the operating needle in real-time.

Reliable and accurate real-time image guidance for vascular access has the potential to appreciably impact public health by enhancing patient safety and convenience, improving procedural accuracy and increasing procedure throughput. Successful implementation has the potential to reduce care and complication costs across millions of vascular access procedures.

Vu-Path™ is a small footprint, US-based device with needle guide. It is a dual-lumen instrument with parallel US imaging and interventional lumens. The forward-viewing US transducer is located at the catheter tip and focused such that the tip of the needle in the interventional lumen, and all proximate structures, are always clearly visualized in real time throughout the procedure.

This is a first-in-human pilot study of the Vu-Path™ device, aiming to its establish clinical feasibility and safety for exemplary use.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: December 2026
• Est. primary completion date: December 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female participants, 18 years of age or older at the time of enrollment.

• Participants meeting all medical conditions for percutaneous angiography.

• International Normalized Ratio (INR) <1.3.

• Written informed consent to participate in the study.

• Ability to comply with the requirements of the study procedures.

Exclusion Criteria:

• Fibrous tissue in access path.

• Active skin infection at the point of needle insertion.

• Hemophilia, thrombocytopenia, coagulopathy, or other elevated risk for bleeding or abnormal clotting

• Use of antithrombotic medication.

• For participants taking warfarin or other anticoagulant medication, INR >1.3.

• Participants who cannot tolerate mild sedation.

• Participants with the following laboratory values, unless approved by hematologist:

Platelet count <100,000/mL, Activated Partial Thromboplastin Time (APTT) >39 sec or Prothrombin Time (PT) >15 sec

• Pregnancy or lactation

• Patient is unable to comply with requirements of the procedure, i.e. holding breath

• Participation in an investigational trial within 30 days of enrollment.

• Any form of substance abuse (including drug or alcohol abuse), psychiatric disorder, or any chronic condition that could, in the opinion of the investigator, of interfering with the conduct of the study.

• Participants who are uncooperative or cannot follow instructions.

Related Conditions & MeSH terms

• Vascular Access

Intervention

Device:
• Vu-Path™
Femoral arterial access in eligible participants will be performed using the Vu-Path™.

Locations

Country	Name	City	State
n/a

Sponsors (3)

Lead Sponsor	Collaborator
Johns Hopkins University	National Heart, Lung, and Blood Institute (NHLBI), Perceptive Navigation LLC

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Device Safety as assessed by number of participants with Minor Bleeding	Device Safety will be assessed by the number of participants experiencing minor bleeding resulting from vascular puncture. Minor bleeding is defined as either a) bleeding that requires no therapy, or has no consequences or, b) requires nominal therapy, or has no consequence or, c) includes overnight admission for observation only.	Within 24 hours from intervention
Primary	Device Safety as assessed by number of participants with Major Bleeding	Device Safety will be assessed by the number of participants experiencing major bleeding. Major bleeding is defined as bleeding that either a) requires therapy and minor hospitalization (25-48 hours) or, b) requires major therapy, unplanned increase in level of care and prolonged hospitalization (> 48 hours), or c) has permanent adverse sequelae or, d) results in death.	Within 3 days from intervention
Secondary	Technical accuracy as assessed by number of attempts to reach target site	Number of attempts to reach target site	Within 1 hour from intervention
Secondary	Technical accuracy as assessed by percentage of first attempt accesses to target site	Percentage of first attempt accesses to target site.	Within 1 hour from intervention
Secondary	Technical efficacy as assessed by procedure time (minutes)	Procedure time is defined as the total time needed for device procedure.	Within 1 hour from intervention
Secondary	Technical efficacy as assessed by target access time (minutes)	Target access time is defined as the total time needed from target visualization to target access.	Within 1 hour from intervention
Secondary	Technical efficacy as assessed by device usage time (minutes)	Device usage time is defined as the total time needed for device use.	Within 1 hour from intervention