Status:

UNKNOWN

Investigation of Plaque Instability Using Bevacizumab-800CW and MSOT

Lead Sponsor:

G.M. van Dam

Conditions:

Atherosclerosis

Carotid Stenosis

Eligibility:

All Genders

21+ years

Phase:

NA

Brief Summary

Determining whether we could visualize uptake of the fluorescent tracer Bevacizumab-800CW, targeting VEGF-A in atherosclerotic plaques by using the new imaging technique Multispectral Optoacoustic Tom...

Detailed Description

Rationale: This project consists of the realization followed by the clinical validation of a procedure dedicated to detect vulnerable atherosclerotic plaques patients with a symptomatic carotid stenos...

Eligibility Criteria

Inclusion

  • Patients above the age of 21 with an indication to undergo a carotid endarterectomy for suspected symptomatic atherosclerotic plaque based on the presence of a CVA and/or transient ischemic attacks (TIA's), including amourosis fugax.
  • Patients with significant and symptomatic carotid stenosis who are scheduled for carotid endarterectomy as decided by the surgeon or the Multi-Disciplinary Carotid Board

Exclusion

  • Medical or psychiatric condition that compromises the patient's ability to give informed consent
  • Pregnant or lactating women
  • Significantrenal(creatinine\>110μmol/L)dysfunction
  • History of iodine allergy or anaphylactic reactions to insect bites or medication or previous allergic reaction to bevacizumab
  • Presence or history of hyperthyroidism

Key Trial Info

Start Date :

April 10 2019

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 1 2020

Estimated Enrollment :

15 Patients enrolled

Trial Details

Trial ID

NCT03757507

Start Date

April 10 2019

End Date

March 1 2020

Last Update

April 12 2019

Active Locations (0)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 0 (0 locations)

No Results Found

We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.