Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

The Pivotal Study of RapidPulseTM Aspiration System

NCT06029491 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trials is to demonstrate the safety and effectiveness for the RapidPulseTM Aspiration System in patients experiencing acute ischemic stroke within 8 hours of symptom onset or last seen normal. Subjects will undergo mechanical thrombectomy (a procedure to remove a clot in the brain which is preventing blood flow), with the RapidPulseTM Aspiration System. Participation in the trial is for 90 days.

Conditions Studied

Interventions

  • DEVICE RapidPulseTM Aspiration System

Study Locations (20)

Florida

  • Baptist Health Research Institute — Jacksonville
  • University of South Florida — Tampa

Illinois

  • Rush University Medical Center — Chicago
  • Advocate Aurora Research Institute — Park Ridge

New York

  • State University of New York at Buffalo — Buffalo
  • Icahn School of Medicine at Mount Sinai — New York

Tennessee

  • Semmes Murphey Foundation - Baptist Memorial Hospital — Memphis
  • Vanderbilt University Medical Center — Nashville

Other

  • Centre Hospitalier Universitaire de Bordeaux — Bordeaux
  • Centre Hospitalier Universitaire de Montpellier — Montpellier

California

  • Providence Saint John's Medical Foundation — Torrance

Connecticut

  • Yale University — New Haven

Georgia

  • Emory University at Grady — Atlanta

Trial Details

FieldValue
Enrollment Target 170 participants
Start Date 2025-03-27
Est. Completion 2027-04
Phase NA

Sponsor

RapidPulse

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06029491

The ClinicalTrials.gov registry entry for NCT06029491 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 170 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is RapidPulse, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acute Ischemic Stroke appearing as the primary indexed condition, and to 1 intervention — of which RapidPulseTM Aspiration System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06029491 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Florida, Illinois, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06029491 about?

NCT06029491 is a clinical study titled "The Pivotal Study of RapidPulseTM Aspiration System". The goal of this clinical trials is to demonstrate the safety and effectiveness for the RapidPulseTM Aspiration System in patients experiencing acute ischemic stroke within 8 hours of symptom onset or last seen normal. Subjects will undergo mechanical thrombectomy (a procedure to remove a clot in th...

What is the current status of trial NCT06029491?

This trial is currently recruiting. It is a NA study. The enrollment target is 170 participants. The study started on 2025-03-27. Estimated completion is 2027-04.

What conditions does trial NCT06029491 study?

This clinical trial studies the following conditions: Acute Ischemic Stroke. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06029491?

The interventions under investigation include: RapidPulseTM Aspiration System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06029491?

This trial is sponsored by RapidPulse, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06029491 being conducted?

This trial has 20 study locations across California, Connecticut, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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