Emergent Large Vessel Occlusion Endovascular Rescue Therapy With Underlying Intracranial Stenosis

Part of paid clinical trials in Toledo, Ohio.

Sponsor
ProMedica Health System
Study ID
NCT07356284
Phase
PHASE3
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Mechanical Thrombectomy plus adjunct stenting — PROCEDURE
    Mechanical thrombectomy and adjunct stentiing
  • Mechanical Thrombectomy — DEVICE
    Mechanical thrombectomy only

Study Details

The study objective is to establish the safety and efficacy of endovascular adjunct stenting for patients undergoing mechanical thrombectomy (MT) that are found to have residual stenosis (70-99%) following attempted clot retrieval with either aspiration catheters or stent retrievers, per device instructions for use and device labeling.

Key Dates

Start date
May 19, 2026
Status verified
Feb 2026
Primary completion
Jun 1, 2030
Completion
Jun 1, 2030

Study Design

Enrollment
342 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Randomized to Mechanical Thrombectomy (MT) plus adjunct Stenting
    Patients will have mechanical thrombectomy (MT) and stenting
  • Active Comparator: Randomized to Mechanical Thrombectomy (MT)
    Patients will only have mechanical thrombectomy (MT) done

Primary Outcome Measure

Primary Efficacy Endpoint [ Time Frame: 90 (+/- 30) days post treatment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
ProMedica Toledo HospitalToledoOhio43606
Kathryn Scalzo
[email protected]
4192914068
Scalzo
Mouhammad Jumaa, MD (PRINCIPAL_INVESTIGATOR)

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