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RECRUITING

The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage Evacuation

NCT04494295 · View on ClinicalTrials.gov ↗

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

14 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04494295

The ClinicalTrials.gov registry entry for NCT04494295 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 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 14 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 Supratentorial Hemorrhage appearing as the primary indexed condition, and to 1 intervention — of which Aurora Surgiscope 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: NCT04494295 reports 20 study locations spanning 16 distinct geographic areas — top geographies include Florida, Missouri, 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 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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04494295?

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

Who is sponsoring clinical trial NCT04494295?

This trial is sponsored by Integra LifeSciences Corporation, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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