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NCT05499832CompletedPhase 3

Safety and Efficacy of Intra-arterial Tenecteplase for Noncomplete Reperfusion of Intracranial Occlusions

Source: ClinicalTrials.gov · Last updated 10 Feb 2026

Brief summary (registry, in English)

TECNO is a multicenter, prospective, randomized, open label, blinded endpoint (PROBE) proof-of-concept trial evaluating if additional administration of intra-arterial Tenecteplase (TNK) improves reperfusion in patients with incomplete mechanical thrombectomy (MT). For this purpose, 156 adult participants experiencing an acute ischemic stroke due to a large vessel occlusion with incomplete reperfusion with residual occlusions after MT will be randomly assigned to receive 3mg intra-arterial (IA) TNK or best medical treatment. Recruitment will occur at 20 academic tertiary stroke care centers in Switzerland, Spain, Belgium, and Germany and patients are followed up for 90 days after the index event. Showing superiority for reperfusion outcomes would have a major impact on the future management of stroke patients.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
156 (actual)
First submitted
26 Apr 2022
Start date
21 Mar 2023
Primary completion date
9 Oct 2025
Lead sponsor
Insel Gruppe AG, University Hospital Bern
Diseases
Stroke
NCT number
NCT05499832

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 156
  • From 21 Mar 2023 to the primary completion date, 9 Oct 2025
  • 51 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Acute intracranial hemorrhage
  • Any severe bleeding within the past 6 months, which would prevent administration of intravenous thrombolysis in clinical routine Major surgery in the past 2 months with severe risk of bleeding, which would prevent administration of intravenous thrombolysis in clinical routine
  • Non-controlled hypertension (defined as SBP \>185 mmHg or DBP \>110 mmHg refractory to treatment)
  • Active dyspeptic ulcer
  • Known neoplasms with risk of bleeding
  • Severe liver fibrosis or portal hypertension
  • Known allergy to TNK or Gentamicin or other additives/auxiliaries (Polysorbatum 20, L-Argininum, Acidum phosphoricum)

Lab values

  • Intake of Vitamin K antagonists with INR \>1.7
  • Platelets \< 50,000
  • Known Renal failure either as defined by a serum creatinine \> 3.0 mg/dl (or 265.2 μmol/l) or glomerular Filtration Rate \[GFR\] \< 30 or as subject who required hemodialysis/peritoneal dialysis

Other

  • Contraindication to MRI (e.g. pacemaker)
  • Known arterial aneurysm
  • Acute pericarditis
  • Acute endocarditis
  • Acute pancreatitis
  • Radiological confirmed evidence of mass effect or intracranial tumor (except small meningioma)
  • Radiological confirmed evidence of cerebral vasculitis
  • Calcified thrombi
  • Pregnancy or lactating women

Who the study is looking for

  • Informed consent
  • Age ≥18 years
  • Clinical signs consistent with an acute ischemic stroke
  • Patient had an initial vessel occlusion in the anterior or posterior circulation defined as intracranial ICA, M1, M2, M3, A1, A2, P1 or P2
  • Patient has undergone endovascular stroke treatment
  • Onset to randomization no later than \< 705 minutes (11h 45min) after symptom-onset/last-seen well.
  • Incomplete reperfusion defined as any of the following:
    • For ICA/M1: TICI2b/2c (50-99%) reperfusion after endovascular treatment without mechanically amendable target-occlusion (as per definition by the interventionalist).
    • For A1/A2, P1/P2, M2/M3: TICI2a/2b/2c (1-99%) reperfusion after endovascular treatment without mechanically amendable target-occlusion (as per definition by the interventionalist).
    • Any emboli to new territory without mechanically amendable target-occlusion (as per definition by the interventionalist).
  • Signs of early ischemic changes of non-contrast CT Alberta Stroke Program Early CT Score (ASPECTS) ≥5 (for DWI-ASPECTS ≥ 4, for DWI-ASECTS: a region must have diffusion abnormality in 20% or more of its volume to be considered DWI-ASPECTS positive)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (51)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
LKH - Universitätsklinikum Graz
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GrazAustriaUnknown status
Medizinische Universität Innsbruck
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InnsbruckAustriaUnknown status
Kepler Universitatsklinikum GmbH
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LinzAustriaUnknown status
Christian-Doppler-Klinik Salzburg
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SalzburgAustriaUnknown status
Hôpital universitaires de Bruxelles
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AnderlechtBelgiumUnknown status
Az Sint-Jan Brugge Av
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BrugesBelgiumUnknown status
Cliniques universitaires Saint-Luc
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BrusselsBelgiumUnknown status
UZ Brussel
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BrusselsBelgiumUnknown status
Universitair Ziekenhuis Gent
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GhentBelgiumUnknown status
UZ Gasthuisberg Leuven
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LeuvenBelgiumUnknown status
Clinique CHC MontLégia
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LiègeBelgiumUnknown status
Kantonsspital Aarau AG
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AarauSwitzerlandUnknown status
Kantonsspital Aarau
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AarauSwitzerlandUnknown status
Universitätsspital Basel
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BaselSwitzerlandUnknown status
Universitatsspital Bern
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BernSwitzerlandUnknown status
Hôpitaux universitaires de Genève
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GenevaSwitzerlandUnknown status
Centre Hospitalier Universitaire Vaudois
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LausanneSwitzerlandUnknown status
Centre Hospitalier Universitaire Vaudois (CHUV)
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LausanneSwitzerlandUnknown status
University Hospital of Lausanne
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LausanneSwitzerlandUnknown status
Kantonsspital Luzern
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LucerneSwitzerlandUnknown status
Ospedale Regionale di Lugano
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LuganoSwitzerlandUnknown status
Kantonsspital St. Gallen
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Sankt GallenSwitzerlandUnknown status
Universitätsspital Zürich
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ZurichSwitzerlandUnknown status
Universitätsklinikum Augsburg
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AugsburgGermanyUnknown status
Universitätsklinikum Bonn
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BonnGermanyUnknown status
Klinikum Bremen-Mitte
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BremenGermanyUnknown status
Universitatsklinikum Carl Gustav Carus An Der Technischen Universitat Dresden
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DresdenGermanyUnknown status
Helios Klinikum Erfurt
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ErfurtGermanyUnknown status
Universitätsklinikum Frankfurt
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FrankfurtGermanyUnknown status
Universitätsklinikum Freiburg
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Freiburg im BreisgauGermanyUnknown status
Universitätsmedizin Göttingen
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GöttingenGermanyUnknown status
Universitätsklinikum Halle (Saale)
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HalleGermanyUnknown status
Universitätsklinikum Hamburg-Eppendorf
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HamburgGermanyUnknown status
Asklepios Klinik Altona
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HamburgGermanyUnknown status
Universitätsklinikum Schleswig-Holstein, Campus Kiel
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KielGermanyUnknown status
Universitätsklinikum Magdeburg A.ö.R.
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MagdeburgGermanyUnknown status
Universitätsmedizin Mannheim
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MannheimGermanyUnknown status
Johannes Wesling Klinikum Minden
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MindenGermanyUnknown status
Klinikum rechts der Isar der Technischen Universität München
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MünchenGermanyUnknown status
Klinikum der Universität München
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MünchenGermanyUnknown status
Universitätsklinikum Münster
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MünsterGermanyUnknown status
Städtisches Klinikum Sollingen
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SolingenGermanyUnknown status
Universitätsklinikum Tübingen
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TübingenGermanyUnknown status
University Hospital Helsinki
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HelsinkiFinlandUnknown status
Amsterdam UMC
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AmsterdamNetherlandsUnknown status
Leiden UMC
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LeidenNetherlandsUnknown status
Hospital de Braga
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BragaPortugalUnknown status
Hospital Nelio Mendonca Funchal
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FunchalPortugalUnknown status
Lisbon Central University Hospital
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LisbonPortugalUnknown status
Hospital Eagas Moniz
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LisbonPortugalUnknown status
Hospital Santo Antonio
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PortoPortugalUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.