Clear-Road Trial, Investigating the Efficacy of the RoadSaver Stent

Last updated: July 31, 2017
Sponsor: Flanders Medical Research Program
Overall Status: Completed

Phase

2/3

Condition

Peripheral Arterial Occlusive Disease

Circulation Disorders

Claudication

Treatment

N/A

Clinical Study ID

NCT02529345
FMRP-130919
  • Ages > 18
  • All Genders

Study Summary

The objective of this clinical investigation is to evaluate the clinical outcome (up to 12 months) of treatment by means of stenting with the RoadSaver (Terumo) in subjects at high risk for carotid endarterectomy requiring carotid revascularization due to significant extra-cranial carotid artery stenosis.

Eligibility Criteria

Inclusion

Inclusion Criteria: High risk for carotid endarterectomy due to anatomical or co-morbid conditions and either:

  • has neurological symptoms and ≥ 50% stenosis via angiography, or

  • is asymptomatic and has ≥ 80% stenosis via angiography.

  1. Target lesion located in the distal common carotid artery (CCA), internal carotidartery (ICA), or carotid bifurcation.

  2. Arterial segment to be stented has a diameter between 4mm and 9mm

  3. Age ≥ 18 years.

  4. Life expectancy > 12 months from the date of the index procedure.

  5. Provides a signed, IRB (Institutional Review Board) / IEC (Institutional EthicalCommittee) approved informed consent form prior to participation.

  6. Willing and able to comply with follow-up requirements.

Exclusion

Exclusion Criteria:

  1. Contra-indication to percutaneous transluminal angioplasty (PTA).

  2. Sever vascular tortuosity or anatomy that would preclude the safe introduction of aguide catheter, sheath, embolic protection system or stent system.

  3. Lesions in the ostium of the common carotid artery.

  4. Occlusion of the target vessel.

  5. Evidence of intraluminal thrombus.

  6. Known sensitivity to nickel-titanium.

  7. Known allergy to heparin, aspirin or other anticoagulant/antiplatelet therapies, or isunable or unwilling to tolerate such therapies.

  8. Uncorrectable bleeding disorders, or will refuse block transfusion.

  9. History of prior life-threatening contrast media reaction.

  10. Previous stent placement in the target vessel.

  11. Evolving stroke or intracranial haemorrhage.

  12. Previous intracranial haemorrhage or brain surgery within the past 12 months.

  13. Clinical condition that makes endovascular therapy impossible or hazardous.

Study Design

Total Participants: 100
Study Start date:
April 01, 2015
Estimated Completion Date:
May 31, 2017

Study Description

It is a Prospective, multi-center, physician-sponsored clinical study.

The objective of this clinical investigation is to evaluate the clinical outcome (up to 12 months) of treatment by means of stenting with the RoadSaver (Terumo) in subjects at high risk for carotid endarterectomy requiring carotid revascularization due to significant extra-cranial carotid artery stenosis.

Connect with a study center

  • Imelda Hospital

    Bonheiden, Antwerp 2820
    Belgium

    Site Not Available

  • OLV Aalst

    Aalst, Oost-Vlaanderen 9300
    Belgium

    Site Not Available

  • AZ Sint-Blasius

    Dendermonde, Oost-Vlaanderen 9200
    Belgium

    Site Not Available

  • RZ Heilig Hart Hospital

    Tienen, 3300
    Belgium

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.