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NCT04494295 · ClinicalTrials.gov registry record

The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage Evacuation

A clinical trial of Supratentorial Hemorrhage, sponsored by Integra LifeSciences Corporation.

Recruiting
Registry status
500
Enrollment target
20
Study locations

NCT04494295 is a study of Supratentorial Hemorrhage that is actively recruiting participants, run by Integra LifeSciences Corporation. The registered enrollment target is 500 participants. The trial reports 20 study locations across 16 states.

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The verdict

NCT04494295, a study of Supratentorial Hemorrhage, is actively recruiting participants, sponsored by Integra LifeSciences Corporation.

RECRUITING
Registry status
500 participants
Enrollment target
20
Study locations

Study Summary

This registry will study the use of the Aurora® Surgiscope to provide surgical access and visualization in minimally invasive removal of hematoma in the brain. Many methods of hematoma removal are available and will be based on surgeon preference. The impact of patient selection and time to surgery from last known well time will be explored.

Conditions Studied

Interventions

  • DEVICE Aurora Surgiscope System

Study Locations (20)

Florida

  • University of Miami - Miami
  • University of South Florida - Tampa

Missouri

  • University of Missouri - Columbia
  • Washington University in St. Louis - St Louis

New York

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

Pennsylvania

  • Pennsylvania State University - Hershey
  • University of Pennsylvania - Philadelphia

California

  • Providence Health - Burbank

Illinois

  • Rush University Medical Center - Chicago

Maryland

  • MedStar Health Research Institute - Baltimore

Michigan

  • Corewell Health - Grand Rapids

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2020-10-23
Est. Completion 2029-10-15

Sponsor

Integra LifeSciences Corporation

60 total trials

What the Registry Record Tells You About NCT04494295

The ClinicalTrials.gov registry entry for NCT04494295 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Integra LifeSciences Corporation, which has 60 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Supratentorial Hemorrhage appearing as the primary indexed condition, and to 1 intervention - of which Aurora Surgiscope System is the first listed.

NCT04494295 reports 20 study locations spanning 16 distinct geographic areas - top geographies include Florida, Missouri, New York.

Frequently Asked Questions

What is clinical trial NCT04494295 about?

NCT04494295 is a clinical study titled "The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage Evacuation". This registry will study the use of the Aurora® Surgiscope to provide surgical access and visualization in minimally invasive removal of hematoma in the brain. Many methods of hematoma removal are available and will be based on surgeon preference. The impact of patient selection and time to surgery ...

What is the current status of trial NCT04494295?

This trial is currently recruiting. The enrollment target is 500 participants. The study started on 2020-10-23. Estimated completion is 2029-10-15.

What conditions does trial NCT04494295 study?

This clinical trial studies the following conditions: Supratentorial Hemorrhage.

What interventions are being tested in trial NCT04494295?

The interventions under investigation include: Aurora Surgiscope System (DEVICE).

Who is sponsoring clinical trial NCT04494295?

This trial is sponsored by Integra LifeSciences Corporation, which has 60 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04494295 being conducted?

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

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.