Establishing Clinical Utility of a New Diagnostic Test in Patients Undergoing Cardiac Catheterization

Qure Healthcare

Status: Completed

Conditions: AKI; Contrast-induced Nephropathy

Treatments: Other: Experimental Arm

Study type: Interventional

Funder types: Industry; Other

Identifiers

NCT04266834

01CMC2019

Details and patient eligibility

About

This study will collect high-quality randomized controlled data across the U.S. from practicing cardiologists performing invasive/interventional procedures and determine how they currently manage patients at risk for CIN and how the results of Hikari's L-FABP test change clinical decision making.

Full description

This study will collect high-quality randomized controlled data across the U.S. from practicing cardiologists performing invasive/interventional procedures and determine how they currently manage patients at risk for CIN and how the results of Hikari's L-FABP test change clinical decision making. Data from this study will better illuminate the clinical use cases with the most significant impact on clinical decision making (and thus the largest potential clinical utility) and the associated physician characteristics (e.g., age, practice setting, training) associated with test adoption.

This study leverages simulated patient cases called Clinical Performance and Value vignettes (CPVs) in a proven methodology to rapidly measure physician care decisions. CPVs are a unique and scalable tool that standardizes practice measurement by having all providers care for the same (virtual) patients. With all providers caring for the same patients, the CPVs generate unbiased data that yields powerful insights into clinical decision making and how these decisions change with the introduction of a new product or solution. Data from the CPVs can quickly demonstrate the clinical utility of a solution, be published in peer-reviewed literature, inform marketing strategies and positively impact coverage and reimbursement decisions.

The study is a prospective cohort trial with six steps:

1. Enrollment: The study will enroll 166 practicing cardiologists who perform invasive or interventional procedures in the U.S. and are determined to be eligible by an eligibility screener.
2. Provider survey: Once providers are enrolled in the study, they will be asked to complete a questionnaire describing their practice and professional background.
3. Randomization: The 166 cardiologists will be randomized into equally-sized (83) control and intervention arms.
4. CPVs (First Round): Physicians will complete three randomly-assigned CPV patient simulations in random order. Cases will be identical across the intervention and control arms. All cases are presented on an online platform, participants are provided with unique weblinks, accessible via any internet-connected computer.
5. Education: The intervention-arm cardiologists will receive educational materials duplicating what physicians would receive in the real-world market as they adopt the L-FABP test. These materials may be comprised of a slide deck, fact sheet, webinar, or case studies.
6. CPVs: Physicians will then complete three additional CPV patient simulations in random order. Cases will be identical across the intervention and control arms, except that the intervention arm will receive L-FABP test results at an appropriate point in each simulated case in the post-intervention round.

Enrollment: 157 patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Board-certified in cardiology for at least two years
2. Averaging at least 20 hours per week of clinical and patient care duties over the last six months
3. Averaging at least one day per month performing invasive or interventional cardiology procedures over the last six months
4. English speaking
5. Access to the internet
6. Informed, signed and voluntarily consented to be in the study

Exclusion criteria

1. Non-English speaking
2. Unable to access the internet
3. Do not voluntarily consent to be in the study

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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157 participants in 2 patient groups

Experimental

Experimental group

Description:

Experimental-arm providers will complete two rounds of three simulated patient cases (CPVs) with two additions described in the next column:

Treatment:

Other: Experimental Arm

Control

No Intervention group

Description:

These providers will complete two rounds of three simulated patient cases (CPVs) only.