Skip to main content
OpenTrials
Completed

NCT Number: NCT05499832

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

LKH-Universitätsklinikum Graz, Graz, Austria

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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)

Exclusion criteria

  • Acute intracranial hemorrhage
  • Contraindication to MRI (e.g. pacemaker)
  • 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
  • Intake of Vitamin K antagonists with INR >1.7
  • Platelets < 50,000
  • Non-controlled hypertension (defined as SBP >185 mmHg or DBP >110 mmHg refractory to treatment)
  • Active dyspeptic ulcer
  • Known arterial aneurysm
  • Known neoplasms with risk of bleeding
  • Severe liver fibrosis or portal hypertension
  • Acute pericarditis
  • Acute endocarditis
  • Acute pancreatitis
  • Known allergy to TNK or Gentamicin or other additives/auxiliaries (Polysorbatum 20, L-Argininum, Acidum phosphoricum)
  • 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
  • Radiological confirmed evidence of mass effect or intracranial tumor (except small meningioma)
  • Radiological confirmed evidence of cerebral vasculitis
  • Calcified thrombi
  • Pregnancy or lactating women

Treatment and study plan

Tenecteplase

Drug

Patients randomized to IA treatment will receive IA TNK via a standard approved microcatheter positioned as close as possible to the residual occlusion site or as distal as possible in the originating vessel if multiple residual occlusions exists.

Primary outcomes

  1. Early reperfusion of the residual intracranial occlusion(s)

    Time frame: 25 minutes after randomization

    Defined by reperfusion improvement on angiography images

  2. Late reperfusion of the residual intracranial occlusion(s)

    Time frame: 24 hours ±6 hours

    Defined by complete reperfusion on perfusion imaging

Secondary outcomes

  1. Degree of disability or dependence assessed by the modified ranking scale (mRS) (shift analysis)

    Time frame: 90 days+/-15 days

    mRS

  2. Normalized change in National Institute of Health Score Scale (NIHSS)

    Time frame: 24 hours +/- 6 hours post-randomization

    NIHSS

  3. Change in National Institute of Health Score Scale (NIHSS)

    Time frame: 90 days +/- 15 days post-randomization

    NIHSS

  4. Quality of life as assessed by the EuroQol 5D-3L (EQ-5D-3L)

    Time frame: 90 days +/- 15 days

    EuroQol 5D-3L

  5. All-cause mortality

    Time frame: 90 days

    Mortality

Sponsors and collaborators

Lead sponsor

Insel Gruppe AG, University Hospital Bern

Other

Registry information

Acronym: TECNO

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Aug 12, 2022
Registry last updated
Feb 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.