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NCT07356284 · ClinicalTrials.gov registry record · Phase 3

Emergent Large Vessel Occlusion Endovascular Rescue Therapy With Underlying Intracranial Stenosis

A Phase 3 study, sponsored by ProMedica Health System.

Recruiting
Registry status
Phase 3
Development phase
342
Enrollment target

NCT07356284 is a Phase 3 study that is actively recruiting participants, run by ProMedica Health System. The registered enrollment target is 342 participants.

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The verdict

NCT07356284, a Phase 3 study, is actively recruiting participants, sponsored by ProMedica Health System.

RECRUITING
Registry status
Phase 3
Development phase
342 participants
Enrollment target

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.

Interventions

  • PROCEDURE Mechanical Thrombectomy plus adjunct stenting
  • DEVICE Mechanical Thrombectomy

Trial Details

FieldValue
Enrollment Target 342 participants
Start Date 2026-05-19
Est. Completion 2030-06-01
Phase Phase 3

Sponsor

ProMedica Health System

12 total trials

What the Registry Record Tells You About NCT07356284

The ClinicalTrials.gov registry entry for NCT07356284 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 342 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ProMedica Health System, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Mechanical Thrombectomy plus adjunct stenting is the first listed.

NCT07356284 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07356284 about?

NCT07356284 is a clinical study titled "Emergent Large Vessel Occlusion Endovascular Rescue Therapy With Underlying Intracranial Stenosis". 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 inst...

What is the current status of trial NCT07356284?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 342 participants. The study started on 2026-05-19. Estimated completion is 2030-06-01.

What interventions are being tested in trial NCT07356284?

The interventions under investigation include: Mechanical Thrombectomy plus adjunct stenting (PROCEDURE), Mechanical Thrombectomy (DEVICE).

Who is sponsoring clinical trial NCT07356284?

This trial is sponsored by ProMedica Health System, which has 12 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.