Skip to main content
OpenTrials
Completed

NCT Number: NCT04055740

Intravascular Ultrasound (IVUS) Imaging During Transvenous Lead Extraction

The purpose of this study is to prospectively evaluate intravascular ultrasound (IVUS) imaging as a tool for grading the presence and characterization of intravascular lead adherence (ILA, or scarring) to cardiovascular implantable electronic device (CIED) leads during transvenous lead extraction (TLE) procedures in a multi-center study. IVUS should identify the location and severity of these adhesions, which the investigators will then correlate to difficulty of the extraction procedure using metrics like pulses of laser energy delivered and time required to traverse an area of fibrosis or ILA. The investigators will be focusing primarily on the section from innominate vein (INNV) down through the superior vena cava (SVC) to the right atrium.

Using IVUS to view blood vessels and the heart structure is approved by the Food and Drug Administration (FDA). Using it as described in this study is off label because of the manner in which it is advanced to the SVC, through the right atrium. While it is not restricted from use in this way, it is not specifically on-label. It should be noted that the use of IVUS during TLE procedures as proposed in this study is routine at the University of Chicago and patients will undergo this procedure regardless of participation in this study. The EP physician team regards the use of IVUS during TLE to be nonsignificant risk.

Completed

Looking for future studies?

Notify Me

Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Chicago

Chicago, Illinois, 60637, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients at least 21 years of age
  • Patients with at least one lead over 1 year dwell time requiring extraction

Exclusion criteria

  • Inability of patient capacity to provide consent for themselves either due to medical or psychiatric comorbidity
  • Venous occlusion to the extent that the IVUS catheter cannot pass
  • Leads < 1 year dwell time requiring extraction

Treatment and study plan

IVUS Imaging

Device

IVUS or radial-ICE (intracardiac echocardiography) is a visualization tool used in many cardiac procedures including electrophysiology procedures (catheter ablation). Its utility in identifying ILA will be assessed in this study.

Primary outcomes

  1. IVUS Grades

    Time frame: 6 hours

    Operators will be able to successfully grade the degree of intravascular lead adherence (ILA) seen using IVUS imaging.

    Using the following scale, grading of ILA in each zone of interest, based on relative motion of lead will be performed:

    i. Grade 1: Freely mobile, Rarely adjacent to vasculature ii. Grade 2: Restricted mobility, Frequently adjacent to vasculature iii. Grade 3: Immobile, Always adjacent to vasculature iv. Grade L, added to number: Lead-to-lead binding

Secondary outcomes

  1. Extraction Difficulty Metrics

    Time frame: Through study completion, expected to be 6 months

    Operators will record the energy and time necessary to traverse binding sites and will be able to correlate these two metrics to IVUS ILA grade

    Extraction difficulty was measured by correlating IVUS ILA grade to lead dwell time - the amount of time it took to extract the lead.

    Using the following scale, grading of ILA in each zone of interest, based on relative motion of lead was performed:

    i. Grade 1: Freely mobile, Rarely adjacent to vasculature ii. Grade 2: Restricted mobility, Frequently adjacent to vasculature iii. Grade 3: Immobile, Always adjacent to vasculature iv. Grade L, added to number: Lead-to-lead binding

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Official study title

Intravascular ultraSound (IVUS) Imaging During transvEnous Lead Extraction (ISEE)

Acronym: ISEE

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Aug 14, 2019
Registry last updated
Sep 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.