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Study identifier: NCT07411079 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Ex Vivo Reproduction of Minimally Invasive Surgery With Hematoma Lysis Using Modified Tissue Plasminogen Activator for Intracerebral Hemorrhage

Condition: Intracerebral Hemorrhage · Hemorrhagic Risk Conditions · Bleeding Disorders  ·  Sponsor: University Hospital, Lille

PhaseN/A
Planned participants1126
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

Intracerebral hemorrhage (ICH) is associated with high mortality and long-term disability, and effective treatment options remain limited. Minimally invasive surgical approaches combined with local administration of thrombolytic agents have been investigated to facilitate hematoma evacuation; however, incomplete clot removal remains frequent, particularly in patients with conditions associated with increased hemorrhagic risk. This observational, cross-sectional study uses an ex vivo model of clinically sized intracerebral hematomas generated from whole blood samples collected from control subjects without hemorrhagic risk and from individuals with predefined hemorrhagic risk profiles, including conditions associated with antithrombotic treatment, inherited bleeding disorders, thrombocytopenia and situations involving reversal or correction of coagulation abnormalities. Using standardized ex vivo hematoma formation and catheter-based administration of modified Tissue Plasminogen Activator (rtPA), the study will characterize clot structure, composition, and permeability across hemorrhagic risk conditions. The study will then determine personalized dosing regimens of modified rtPA in conditions where thrombolytic activity differs from reference values observed in healthy control samples treated with a standard dose. Finally, the thrombolytic activity of personalized dosing regimens will be evaluated by measuring hematoma weight reduction 9 hours after treatment and compared wi…

This description comes directly from the study's public registry record.

Talk to the study team

Mélanie DANIEL, MD  ·  +33 3 20 44 48 42  ·  melanie.daniel@chu-lille.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU de LilleLille, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07411079