Clinical Trial

Non-invasive Ultrasound and Hematoma Clearance After Intracerebral Hemorrhage

Study acronym: NOTICE
Recruiting
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Summary
Intracerebral hemorrhage (ICH) is one of the stroke subtypes with the highest global rates of disability and mortality, accounting for 15%-20% of all strokes. Currently, there is a lack of evidence-based interventions for ICH, with treatment primarily relying on supportive care. There is an urgent clinical need to explore new strategies and technologies. The investigators hypothesize that for ICH patients, best medical treatment combined with a non-invasive ultrasonic scalpel (ultrasound Doppler flow analyzer) may be superior to best medical treatment alone. The primary objective of this study is to determine the safety and efficacy of the non-invasive ultrasonic scalpel in promoting hematoma clearance in ICH patients.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-11-17.
Status change: Not Yet Recruiting → Recruiting 2026-04-14
Trial Details
NCT Number NCT07246473
Lead Sponsor Beijing Tiantan Hospital
Conditions Intracerebral Hemorrhage
Enrollment 86 participants
Start Date 2025-12-12
Primary Completion 2027-08-30 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-17