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Not yet recruiting NCT06696131

Tenecteplase (TNK) in the Treatment of Intracerebral Hemorrhage (ICH)

Phase I Interventional Intracerebral Hemorrhage Intracranial Hemorrhages Hemorrhagic Strokes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: TNK.
Who it may be relevant to
Registry conditions: Intracerebral Hemorrhage, Intracranial Hemorrhages, Hemorrhagic Strokes. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The overall purpose of this study is to look at the safety and effectiveness of administering Tenecteplase (TNK) into the brain bleed (hematoma) instead of another clot-dissolving drug known as recombinant tissue plasminogen activator (rtPA), which is the current standard practice. Clot dissolving (Fibrinolytic) drugs work to break down blood clots and have been found to improve health outcomes when applied directly into the hematoma within the brain. Patients who take part in this study will undergo the same surgical procedure that would normally be performed to treat them, but with the exception of TNK not rtPA.

Interventions

  • Drug TNK
    TNK will be delivered into the site of the intracerebral hemorrhage via a brain catheter.

Primary outcome measures

  • Safety Assessment [Time frame: From treatment until follow-up date (+/- 30 days)]
  • Adverse Event Evaluation [Time frame: From treatment until follow-up date (+/- 30 days)]
Secondary outcome measures (1)
  • Radiological Assessment of the Hematoma Resolution [Time frame: From treatment until follow-up date (+/- 30 days)]

Eligibility criteria

Inclusion criteria

  • Patient/legally authorized representative has signed the Informed Consent Form.
  • Ability to comply with the study protocol, in the investigator's judgment.
  • Patients 18 to 80 years of age with an ICH had occurred within 24 hours before admission.
  • Spontaneous supratentorial (basal ganglia, thalamus, lobar) ICH ≥30 mL measured utilizing the ABC/2 method.
  • Subjects with a GCS score of 5-14.
  • NIHSS ≥6.
  • Stability CT scan done at least 6 hours after baseline CT showing clot stability (growth <5 mL as measured by ABC/2 method). If the hematoma volume measured on the stability CT scan increases by 5 mL or more, a second stability CT scan will be performed 12 hours later.
  • Sustained systolic blood pressure (SBP) <180 mm Hg for six hours recorded closest to the time of drug administration.
  • Symptoms must be present less than 24 hours prior to baseline CT scan.
  • Baseline Rankin score of 0 or 1.

Exclusion criteria

  • Presence of infratentorial parenchymal bleeding.
  • Presence of a hemorrhage extending to the midbrain.
  • An unknown time of onset or the symptoms onset more than 24 hours prior to admission.
  • Pregnancy.
  • Inability to obtain written informed consent from subject or legal representative.
  • Sustained SBP >180 mm Hg for six hours recorded closest to the time of drug administration.
  • Age <18 and >80 years.
  • Radiological evidence of arterio-venous malformation, aneurysm, amyloid angiopathy, Moyamoya disease, hemorrhagic conversion of an ischemic stroke, recurrent hemorrhage in the same location within the past 365 year or unstable mass as a source for the ICH.
  • Evidence of coagulopathy (international normalized ratio >1.3; platelet count <100 ,000 or platelet dysfunction P2Y-12 >250) or known clotting disorder.
  • Bilateral fixed, dilated pupils indicating irreversible impaired brain stem function with GCS ≤4.
  • Patients with severe ICH and IVH who require an external ventricular drain (EVD) placement for cerebrospinal fluid (CSF) diversion or separate intraventricular thrombolysis.
  • Inability to maintain INR less than 1.3.
  • Use of anticoagulants prior to symptom onset and subjects requiring long-term anticoagulants (the reversal is permitted if the patient can tolerate the short-term risk of reversal).
  • Use of Dabigatran, Apixaban, and/or Rivaroxaban (or a similar medication from the similar medication class) prior to symptom onset.
  • Internal bleeding (GI, renal, respiratory etc).
  • Mechanical heart valve (Bioprosthetic heart valve is permitted).
  • Known risk for embolization, including history of left heart thrombus, mitral stenosis with atrial fibrillation, acute pericarditis, or subacute bacterial endocarditis (atrial fibrillation without mitral stenosis is permitted).
  • Allergy or sensitivity to TNKase.
  • Participation in a concurrent clinical trial.
  • Serious illness (advanced stage which can interfere with the outcome).
  • The patient is unstable and would not benefit from a surgical intervention.
  • GCS score of 3-4 and 15 (to ensure patient safety and study feasibility).
  • Historical mRS score of 2-6 (at admission).
  • Symptomatic tract hemorrhage or a tract hemorrhage more than 5 mm.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06696131 · Pro2024001604

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗