Rapid Evacuation and Access of Cerebral Hemorrhage Registry: observing minimally invasive surgery outcomes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational registry collects real-world data on patients with acute spontaneous supratentorial intracerebral hemorrhage who undergo minimally invasive surgical interventions. It aims to quantify outcomes such as functional status and recovery after MIS in the early period following hemorrhage. The study does not assign treatments but records procedures, timing, imaging findings, and outcomes to understand patterns and potential benefits. Eligible patients have hemorrhages of 20 mL or more and receive MIS within seven days, with outcomes analyzed within the registry framework. The investigation is sponsored by Emory University with support from The Marcus Foundation and is conducted at Grady Memorial Hospital in Atlanta, GA.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Head CT demonstrating an acute, spontaneous, intracerebral hemorrhage
* Hemorrhage volume ≥ 20 mLs
* Minimally invasive surgical intervention performed within 7 days of hemorrhage

Exclusion Criteria:

* Ruptured aneurysm, arteriovenous malformation (AVM), vascular anomaly, moyamoya disease, venous sinus thrombosis, mass or tumor, hemorrhagic conversion of an ischemic infarct, recurrence of a recent ICH (\<1 year), as diagnosed with radiographic imaging
* Infratentorial intraparenchymal hemorrhage, including midbrain, pontine, or cerebellum
* Initial hospital arrival ≥ 24 hours after the onset of stroke symptoms
* Last known normal is unknown
* Historical Modified Rankin Score \> 4
* Known life-expectancy of less than 1 year prior to ICH
* DNR or comfort measures only
* Known pregnancy in female subjects
* Inability or unwillingness of subject or legal guardian/representative to give written informed consent within 7 days of initial hospital arrival
* Inability to meet follow up requiremen

Where it's running

• Grady Memorial Hospital
  Atlanta, Georgia, United States Recruiting

Study contacts

• Principal investigator: Alex Hall, DHSc — Emory University
• Study coordinator: Alex Hall, DHSc
• Email: alex.hall@emory.edu
• Phone: 404-778-1585

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals

  This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.

  Recruiting at 2 sites Hospital Universitari Vall d'Hebron Research Institute · Leuven and 6 other locations · NCT07924371

• Smartphone-based EEG to detect hidden awareness in ICU patients with brain injuries

  Researchers will test a smartphone-enabled EEG to see if it can reveal Cognitive Motor Dissociation in ICU patients who can’t show commands at bedside.

  Recruiting Columbia University · Miami, Florida and 8 other locations · NCT07917728

• Chinese multicenter group studies spontaneous intracerebral hemorrhage in adults

  This study tests how a large group of adults with spontaneous intracerebral hemorrhage (and a healthy control group) progress over time to understand outcomes and determinants of recovery.

  Recruiting Xiangya Hospital of Central South University · Changsha, Hunan · NCT07833410

• Single triple-combination blood pressure pill after intracerebral hemorrhage

  This trial tests whether a single pill combining amlodipine, valsartan, and hydrochlorothiazide helps adults who recently had an intracerebral hemorrhage control their blood pressure.

  Recruiting The University of Hong Kong · Hong Kong, Hong Kong and 3 other locations · NCT07458880

• Vitamin D treatment after intracerebral hemorrhage

  This will try giving higher-dose vitamin D to adults within 96 hours of an intracerebral hemorrhage to see if it helps clear the bleed faster and is safe.

  Recruiting The University of Hong Kong · Hong Kong · NCT07458815

• Prototype CT tools for minimally invasive intracerebral hemorrhage evacuation

  This project will test two Siemens prototype CT tools—a perfusion feature and an automatic hemorrhage detector—to see if they help doctors planning and performing minimally invasive brain-bleed (intracerebral hemorrhage) evacuation in adults.

  Recruiting Icahn School of Medicine at Mount Sinai · New York, New York · NCT07455201

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.