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NCT05113381 · ClinicalTrials.gov registry record · NA

The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the Treatment of Intraventricular Hemorrhage (IVH)

A NA study, sponsored by Integra LifeSciences Corporation.

Completed
Registry status
NA
Development phase
105
Enrollment target

NCT05113381: Completed NA study, sponsored by Integra LifeSciences Corporation.

NCT05113381 is a NA study that has completed, run by Integra LifeSciences Corporation. The registered enrollment target is 105 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05113381, a NA study, has completed, sponsored by Integra LifeSciences Corporation.

COMPLETED
Registry status
NA
Development phase
105 participants
Enrollment target

Study Summary

The primary goal of this study is to assess the occurrence of flushing interventions to address occlusions during the treatment of interventricular hemorrhage (spontaneous primary IVH or secondary IVH due to ruptured aneurysm).

Primary Outcome

The number of flushing interventions from initial catheter placement through catheter removal, an average of 10 days, to address occlusions.

Interventions

  • DEVICE CerebroFlo™ EVD Catheter

Trial Details

FieldValue
Enrollment Target 105 participants
Start Date 2021-09-15
Est. Completion 2025-07-31
Phase NA
Integra LifeSciences Corporation

60 total trials

What the finished NCT05113381 record still lists

NCT05113381 is an interventional study that assigns participants to a tested intervention. The registered 105 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which CerebroFlo™ EVD Catheter is the first listed.

NCT05113381 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05113381 about?

NCT05113381 is a clinical study titled "The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the Treatment of Intraventricular Hemorrhage (IVH)". The primary goal of this study is to assess the occurrence of flushing interventions to address occlusions during the treatment of interventricular hemorrhage (spontaneous primary IVH or secondary IVH due to ruptured aneurysm).

What is the current status of trial NCT05113381?

This trial is currently completed. It is a NA study. The enrollment target is 105 participants. The study started on 2021-09-15. Estimated completion is 2025-07-31.

What interventions are being tested in trial NCT05113381?

The interventions under investigation include: CerebroFlo™ EVD Catheter (DEVICE).

Who is sponsoring clinical trial NCT05113381?

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

How this trial's enrollment target compares

Where NCT05113381's enrollment target sits among peer trials

105 834th of 2000 higher than 1,165 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 NCT05113381, the US trial registry maintained by the National Library of Medicine. NCT05113381 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.