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Study identifier: NCT06868511 Synced from ClinicalTrials.gov · July 29, 2026
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Neuronavigation-assisted Stereotactic Puncture With Tenecteplase for Acute Intracerebral Hemorrhage

Condition: Deep Intracerebral Hemorrhage (ICH)  ·  Sponsor: Beijing Tiantan Hospital

PhasePhase 3
Planned participants732
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Background Minimally invasive puncture surgery followed by thrombolysis has been proven to be an effective approach for managing hypertensive intracerebral hemorrhage. Nevertheless, its impact on improving neurological outcomes remains controversial. The integration of neuronavigation-assisted stereotactic (NAS) technology will significantly help enhance the accuracy of catheter placement, while tenecteplase (TNK), a third-generation thrombolytic agent, with greater potency in lysing platelet-rich clots and heightened specificity for fibrin may improve thrombolysis efficiency. However, the efficacy and safety of combining NAS minimally invasive puncture combined with TNK in reducing disability and mortality rates among patients with acute spontaneous deep intracerebral hemorrhage remain unknown. Aim To evaluate the efficacy and safety of neuronavigation-assisted stereotactic MIPS combined with TNK thrombolysis (NAS-TNK)in reducing disability and mortality in patients with deep hypertensive intracerebral hemorrhage. Design NAS-TNK is a randomized, open-label, outcome-blinded multicenter trial, involving 732 participants with acute basal ganglia or thalamic hemorrhage with a hematoma volume ranging from 20-50 mL. This study will evaluate the efficacy and safety of NAS minimally invasive puncture combined with TNK, administered every 24 hours at a dose of 0.009 mg per milliliter of hematoma volume, compared to participants receiving standard medical care. All patients will be …

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

Talk to the study team

Yong Cao  ·  +86 13601362306  ·  caoyong@bjtth.org

Zhiyou Wu  ·  15880085161  ·  786392247@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Beijing Tiantan HospitalBeijing, China, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06868511