PET Imaging of Natriuretic Peptide Receptor C (NPR-C) in Carotid Atherosclerosis

Sponsor
Washington University School of Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT02417688
Collaborator
(none)
22
1
1
81.1
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Study Details

Study Description

Brief Summary

To demonstrate feasibility of imaging Cu[64]-25%-CANF-Comb uptake in the atherosclerosis of the carotid artery of patients for whom carotid artery endarterectomy surgery is planned in comparison to the carotid artery for which intervention is not planned.

Condition or Disease Intervention/Treatment Phase
  • Device: Cu[64]-25%-CANF-Comb PET-MR
Phase 2/Phase 3

Detailed Description

This study is a single center, open-label baseline controlled imaging study designed to demonstrate feasibility of PET imaging of radiopharmaceutical nanoparticle Cu[64]-25%CANF-Comb uptake by PET-MR. Patients will undergo Cu[64]-25%CANF-Comb PET-MR imaging of both carotid arteries. Both carotid arteries will be imaged at the same time. We hope to demonstrate differences in PET SUV (Standardized Uptake Value) in the significantly atherosclerotic artery in patients who will be going to carotid endarterectomy surgery in comparison to the PET SUV in the artery that is not significantly diseased (ie; the artery that will not undergo surgery) . We also will determine whether PET SUV of the Cu[64]-25%CANF-Comb by the plaque correlates to the American Heart Association classifications of atherosclerosis and tissue presence of NPR-C in the ex vivo carotid endarterectomy specimen post surgery as measured by RT-PCR.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
PET-MR Imaging of Natriuretic Peptide Receptor C (NPR-C) in Carotid Atherosclerosis With [64]Cu-25%CANF-Comb
Actual Study Start Date :
Apr 1, 2015
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cu[64]-25%-CANF-Comb PET-MR

Single IV injection of 4-8 mCi of Cu[64]-25%-CANF-Comb with a mass no more than 100 μgrams followed by PET-MR Imaging

Device: Cu[64]-25%-CANF-Comb PET-MR
Single IV injection of a novel radiopharmaceutical for diagnostic imaging of atherosclerosis by PET-MR
Other Names:
  • Cu[64]-25%-CANF-Comb
  • Outcome Measures

    Primary Outcome Measures

    1. PET SUV (Standardized Uptake Value) [22-26 hours]

      Difference in SUV between the carotid with atherosclerosis (carotid artery to be undergo surgery) and the carotid artery without significant disease (artery for which surgery is not planned).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with carotid atherosclerosis

    • Patients must be scheduled for carotid intervention (endarterectomy surgery)

    • Signed informed consent.

    Exclusion Criteria:
    • Unstable clinical conditions

    • Pregnancy and lactation

    • Inability to lie still for up to 60 min with arms down at sides for PET-MR imaging

    • Unwilling to comply with study procedures and unavailable for the duration of the study.

    • Pacemakers, brain aneurysm clip, shrapnel and other typical contraindications for MRI imaging.

    • Inability to provide written informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Washington University in St.Louis Saint Louis Missouri United States 63110

    Sponsors and Collaborators

    • Washington University School of Medicine

    Investigators

    • Principal Investigator: Pamela K Wooderd, MD, Washington University School of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Washington University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT02417688
    Other Study ID Numbers:
    • 201409006
    First Posted:
    Apr 16, 2015
    Last Update Posted:
    Jun 10, 2021
    Last Verified:
    Jun 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Washington University School of Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 10, 2021