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NCT01657461 · ClinicalTrials.gov registry record · NA

Solitaire™ With the Intention For Thrombectomy as PRIMary Endovascular Treatment (SWIFT PRIME) Trial

A NA study of Acute Ischemic Stroke, sponsored by Medtronic Neurovascular Clinical Affairs.

Completed
Registry status
NA
Development phase
196
Enrollment target
1
Study location

NCT01657461 is a NA study of Acute Ischemic Stroke that has completed, run by Medtronic Neurovascular Clinical Affairs. The registered enrollment target is 196 participants, below the 344-participant average among 25 other Acute Ischemic Stroke trials with a reported enrollment target (43% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01657461, a NA study of Acute Ischemic Stroke, has completed, sponsored by Medtronic Neurovascular Clinical Affairs.

COMPLETED
Registry status
NA
Development phase
196 participants
Enrollment target
1
Study location

Study Summary

The primary study objective is to determine if subjects experiencing an acute ischemic stroke due to large vessel occlusion, treated with combined IV t-PA and Solitaire Revascularization Device within 6 hours of symptom onset have less stroke-related neurological disability (mRS) than those subjects treated with IV t-PA alone

Conditions Studied

Interventions

  • DRUG Intravenous (IV) recombinant human tissue plasminogen activator (rtPA)
  • DEVICE Solitaire revascularization device

Study Locations (1)

New York

  • Kaleida Health/Buffalo General - Buffalo

Trial Details

FieldValue
Enrollment Target 196 participants
Start Date 2012-12
Est. Completion 2015-01
Phase NA

What the Registry Record Tells You About NCT01657461

The ClinicalTrials.gov registry entry for NCT01657461 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 196 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 344-participant average among 25 other Acute Ischemic Stroke trials with a reported enrollment target (43% lower). The listed sponsor is Medtronic Neurovascular Clinical Affairs, which has 20 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acute Ischemic Stroke appearing as the primary indexed condition, and to 2 interventions - of which Intravenous (IV) recombinant human tissue plasminogen activator (rtPA) is the first listed.

NCT01657461 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01657461 about?

NCT01657461 is a clinical study titled "Solitaire™ With the Intention For Thrombectomy as PRIMary Endovascular Treatment (SWIFT PRIME) Trial". The primary study objective is to determine if subjects experiencing an acute ischemic stroke due to large vessel occlusion, treated with combined IV t-PA and Solitaire Revascularization Device within 6 hours of symptom onset have less stroke-related neurological disability (mRS) than those subjects...

What is the current status of trial NCT01657461?

This trial is currently completed. It is a NA study. The enrollment target is 196 participants. The study started on 2012-12. Estimated completion is 2015-01.

What conditions does trial NCT01657461 study?

This clinical trial studies the following conditions: Acute Ischemic Stroke.

What interventions are being tested in trial NCT01657461?

The interventions under investigation include: Intravenous (IV) recombinant human tissue plasminogen activator (rtPA) (DRUG), Solitaire revascularization device (DEVICE).

Who is sponsoring clinical trial NCT01657461?

This trial is sponsored by Medtronic Neurovascular Clinical Affairs, which has 20 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01657461 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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