Clinical Trial

Rapid Evacuation and Access of Cerebral Hemorrhage Trial

Study acronym: REACH
Recruiting
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Summary
The main purpose of this study is to compare patients with a deep bleed in the brain undergoing surgery to patients receiving routine medical care. The standard treatment involves admission to the Intensive Care Unit (ICU) with close monitoring and blood pressure control. It also includes other medical (non-surgical) treatments to prevent more bleeding or another stroke. Sometimes, doctors will recommend surgery to remove the blood if medical treatment alone is not successful. There is evidence that doing minimally invasive surgery early-using a small opening in the skull to remove blood-may help some patients. Researchers aim to understand whether this surgery is better than current medical treatment, which may include surgeries to relieve pressure on the brain in some cases. This study, called REACH, is comparing usual medical care to early minimally invasive surgery so doctors can know which is better for patients.
Protocol Amendment History 1 change
notable Trial sites expanded: 21 -> 24 locations 2026-08-15
Trial Details
NCT Number NCT06870812
Lead Sponsor Emory University
Collaborators: The Marcus Foundation
Conditions Stroke Hemorrhagic
Enrollment 600 participants
Start Date 2025-05-27
Primary Completion 2030-03 (estimated)
Study Completion 2030-03 (estimated)
Updated on ClinicalTrials.gov 2026-08-14