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NCT01971359 · ClinicalTrials.gov registry record

Clinical Outcomes Following Parafascicular Surgical Evacuation of Intracerebral Hemorrhage: A Pilot Study

A clinical trial, sponsored by OSF Healthcare System.

Completed
Registry status
2
Enrollment target

NCT01971359: Completed study, sponsored by OSF Healthcare System.

NCT01971359 is a clinical trial that has completed, run by OSF Healthcare System. The registered enrollment target is 2 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01971359 has completed, sponsored by OSF Healthcare System.

COMPLETED
Registry status
2 participants
Enrollment target

Study Summary

This study is determining the clinical outcomes, based on neurological testing, for the parafascicular minimally invasive clot evacuation technique. We will collect data from the time of surgery up until 90 days post procedure. We will also be looking at financial data as well. * H(0): there is no economic benefit to the system with early surgical intervention for ICH * Alternative Hypothesis:H(1) Assuming clinical equipoise, i.e., no benefit in clinical outcome with early surgical intervention (null hypotheses) H(0) is correct), the ability to accelerate the patients care from the entry point to the exit point will result in a significant economic advantage to the system through cost reduction.

Primary Outcome

The primary objective is to compare the 30 day and 90 day clinical outcomes of patients who will undergo parafascicular ICH-evacuation procedure compared to historical outcomes (surgical and non-surgical).

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2013-09
Est. Completion 2014-10
OSF Healthcare System

14 total trials

What the finished NCT01971359 record still lists

NCT01971359 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 2 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT01971359 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01971359 about?

NCT01971359 is a clinical study titled "Clinical Outcomes Following Parafascicular Surgical Evacuation of Intracerebral Hemorrhage: A Pilot Study". This study is determining the clinical outcomes, based on neurological testing, for the parafascicular minimally invasive clot evacuation technique. We will collect data from the time of surgery up until 90 days post procedure. We will also be looking at financial data as well. * H(0): there is no ...

What is the current status of trial NCT01971359?

This trial is currently completed. The enrollment target is 2 participants. The study started on 2013-09. Estimated completion is 2014-10.

Who is sponsoring clinical trial NCT01971359?

This trial is sponsored by OSF Healthcare System, which has 14 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01971359, the US trial registry maintained by the National Library of Medicine. NCT01971359 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.