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NCT02661672 · ClinicalTrials.gov registry record · NA

INVEST-REGISTRY: Minimally Invasive Endoscopic Surgical Treatment With Apollo/Artemis in Patients With Brain Hemorrhage

A NA study of Intracranial Hemorrhage, sponsored by J. Moc.

Completed
Registry status
NA
Development phase
38
Enrollment target
7
Study locations

NCT02661672: Completed NA study of Intracranial Hemorrhage, sponsored by J. Moc.

NCT02661672 is a NA study of Intracranial Hemorrhage that has completed, run by J. Moc. The registered enrollment target is 38 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). The trial reports 7 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02661672, a NA study of Intracranial Hemorrhage, has completed, sponsored by J. Moc.

COMPLETED
Registry status
NA
Development phase
38 participants
Enrollment target
7
Study locations

Study Summary

Objective: The primary objective of this multicenter prospective registry is to provide additional safety, technical outcomes and clinical outcomes data for minimally invasive endoscopic surgery (MIES) with Apollo or Artemis for the evacuation of supratentorial brain hemorrhage in adult patients who do not qualify for the concurrent INVEST Feasibility randomized controlled trial at active INVEST centers.

Primary Outcome

Clinical Efficacy Endpoint: global disability assessed via the modified Rankin score (mRS). 180-day global disability assessed via the modified Rankin score (mRS), categorized as either mRS ≤ 3 or mRS \> 3

Conditions Studied

Interventions

  • DEVICE Apollo Device
  • DEVICE Artemis Device

Study Locations (7)

New York

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

District of Columbia

  • George Washington University - Washington D.C.

Kentucky

  • University of Louisville - Louisville

Pennsylvania

  • Geisinger Medical Center - Danville

South Carolina

  • Prisma Health - Greenville

Washington

  • University of Washington - Seattle

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2016-10-14
Est. Completion 2022-11-16
Phase NA
J. Moc

1 total trials

What the finished NCT02661672 record still lists

NCT02661672 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Intracranial Hemorrhage appearing as the primary indexed condition, and to 2 interventions - of which Apollo Device is the first listed.

NCT02661672 lists 7 locations in 6 states (New York, District of Columbia, Kentucky).

Frequently Asked Questions

What is clinical trial NCT02661672 about?

NCT02661672 is a clinical study titled "INVEST-REGISTRY: Minimally Invasive Endoscopic Surgical Treatment With Apollo/Artemis in Patients With Brain Hemorrhage". Objective: The primary objective of this multicenter prospective registry is to provide additional safety, technical outcomes and clinical outcomes data for minimally invasive endoscopic surgery (MIES) with Apollo or Artemis for the evacuation of supratentorial brain hemorrhage in adult patients who...

What is the current status of trial NCT02661672?

This trial is currently completed. It is a NA study. The enrollment target is 38 participants. The study started on 2016-10-14. Estimated completion is 2022-11-16.

What conditions does trial NCT02661672 study?

This clinical trial studies the following conditions: Intracranial Hemorrhage.

What interventions are being tested in trial NCT02661672?

The interventions under investigation include: Apollo Device (DEVICE), Artemis Device (DEVICE).

Who is sponsoring clinical trial NCT02661672?

This trial is sponsored by J. Moc, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02661672 being conducted?

This trial has 7 study locations across District of Columbia, Kentucky, New York, Pennsylvania, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Intracranial Hemorrhage

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02661672's enrollment target sits among peer trials

38 1538th of 2000 higher than 461 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02661672, the US trial registry maintained by the National Library of Medicine. NCT02661672 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.