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Emergent Large Vessel Occlusion Endovascular Rescue Therapy With Underlying Intracranial Stenosis

NCT07356284 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 342

Last updated 2026-05-22

No results posted yet for this study

Summary

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.

Conditions

  • Brain Stroke
  • Stenting Treatment
  • Acute Ischemic Stroke

Interventions

PROCEDURE

Mechanical Thrombectomy plus adjunct stenting

Mechanical thrombectomy and adjunct stentiing

DEVICE

Mechanical Thrombectomy

Mechanical thrombectomy only

Sponsors & Collaborators

  • ProMedica Health System

    lead OTHER

Principal Investigators

  • Sami Al Kasab, MD · Medical University of South Carolina

  • Mouhammad Jumaa, MD · ProMedica Toledo Hospital

  • Tanya Siddiqui · ProMedica Health System

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-19
Primary Completion
2030-06-01
Completion
2030-06-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07356284 on ClinicalTrials.gov