FAZA PET/MRI in CLI Patients Pre and Post Revascularization

Sponsor
University Health Network, Toronto (Other)
Overall Status
Recruiting
CT.gov ID
NCT04054609
Collaborator
(none)
40
1
1
39
1

Study Details

Study Description

Brief Summary

Peripheral artery disease is a worldwide problem, leading to high mortality and mobility.

Critical limb ischemia (CLI) is associated with high risk of amputation with the subsequent decreased in life quality. Endovascular therapy is now considered the primary treatment option in these patients to improve the vascularity and prevent amputations.

In recent years, development of molecular imaging tools are now become available. A recent radio tracer named 18F-Fluoroazomycin Arabinoside (FAZA) its an specific marker of hypoxia in the tissues and has been used in multiples studies. This tracer can be used in PET/MR scan providing a potentially power diagnostic tool in patients with CLI, allowing in one diagnostic study the evaluation of location and degree of hypoxia in the extremity tissues. This diagnostic tool may offer a better assessment pre and post standard of care endovascular treatment for the patients.

Moreover, some of the patients treated with endovascular therapy may not have a favorable outcome, without a clear reason explaining this situation. We will try to find some predictor model in the FAZA PET/MR that can explain the different outcomes and may help clinicians choose the best treatment option in specific cases.

Thirdly, post processing for optimization of the MR sequences in patients with CLI will be performed at the MR component of the PET. There would thus be great clinical interest in developing non-invasive tools that could provide more accurate diagnostic information compared to traditional tests for these patients population.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: FAZA PET/MRI scan
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
FAZA PET/MRI scan pre and post standard of care endovascular treatment for critical limb ischemia patientsFAZA PET/MRI scan pre and post standard of care endovascular treatment for critical limb ischemia patients
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Evaluation Of Prognostic Value of 18f-Fluoroazomycin Arabinoside (FAZA) Positron Emission Tomography/Magnetic Resonance Imaging (PET/MR) In Patients With Critical Limb Ischemia Pre- and Post Revascularization: a Pilot Study
Actual Study Start Date :
Aug 31, 2019
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: FAZA PET/MRI scan

PET/MRI scan using radiotracer 18F-Fluoroazomycin Arabinoside

Diagnostic Test: FAZA PET/MRI scan
PET/MRI scan using radio tracer named 18F-Fluoroazomycin Arabinoside (FAZA) pre and post standard of care endovascular treatment for critical limb ischemia patients

Outcome Measures

Primary Outcome Measures

  1. Validation of FAZA PET/MRI as a biomarker of hypoxia [FAZA PET/MRI 2-3 weeks before endovascular treatment and 4-6 weeks after endovascular treatment]

    The change of degree and pattern of 18F-Fluoroazomycin Arabinoside (FAZA) uptake in the PET/MRI scan of limb in patients with critical limb ischemia

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age >= 18 years;

  • Patients with clinical evidence of critical limb ischemia that are candidates for revascularization treatment;

  • A negative urine or serum pregnancy test in women of child-bearing age;

  • Ability to provide written informed consent to participate in the study.

Exclusion Criteria:
  • Contraindication for MR as per current institutional guidelines;

  • Inability to lie supine for at least 30 minutes;

  • Pregnant or breastfeeding;

  • Unable or unwilling to provide informed consent;

  • Impending amputation within 6 weeks of presentation;

  • Previous metallic hardware in the lower limbs;

  • Unable to have ethanol.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Health Network Toronto Ontario Canada M5G 2N2

Sponsors and Collaborators

  • University Health Network, Toronto

Investigators

  • Principal Investigator: Patrick Veit-Haibach, MD, University Health Network, Toronto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Health Network, Toronto
ClinicalTrials.gov Identifier:
NCT04054609
Other Study ID Numbers:
  • 18-6114
First Posted:
Aug 13, 2019
Last Update Posted:
Nov 12, 2020
Last Verified:
Nov 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 12, 2020