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Completed

NCT Number: NCT03634748

Thrombolysis in stRoke With Unknown onSet Based on noncontrasT CT

Multicentric, observational, registry-based study of 0.9 mg/kg i.v. thrombolysis in wake-up stroke or stroke with unknown onset based on non-contrast CT appearance only

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

St. Johns Hospital Vienna, Vienna, Austria

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About this study

Thrombolysis in wake-up stroke (WUS) or stroke with unknown onset (SUO) has been recently proven to be safe and effective using magnetic resonance imaging (MRI). However, in most of the thrombolyzing hospitals worldwide MR imaging is not available. We hypothesize that pragmatic non-contrast CT (NCCT)-based WUS/SUO thrombolysis may be feasible and safe.

Methods: TRUST-CT is an international multicenter registry-based study. WUS/SUO patients undergoing NCCT-based thrombolysis with NIHSS ≥ 4 and initial ASPECTS ≥ 7 are included and compared to propensity score matched non-thrombolyzed WUS/SUO controls. Primary endpoint is symptomatic intracranial hemorrhage (ICH); secondary endpoints include 24-hour NIHSS change of ≥ 4 and modified Rankin Score (mRS) at 90 days.

Who can participate

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

Inclusion:

  • Ischemic stroke with NIHSS ≥ 4
  • Wake-up stroke or unknown onset stroke
  • Age ≥ 18 years
  • rtPA Bolus within 4.5h of awakening and/or within 4.5 of discovering symptoms
  • rtPA Bolus within 30 min. of admission CT

Exclusion:

  • Noncontrast cranial CT scan with ASPECTS < 7
  • Evidence of intracranial or subarachnoid hemorrhage
  • Inability to control systolic BP >185mm Hg, or diastolic BP >110mm Hg with IV antihypertensive medication
  • Known coagulopathy or evidence of active bleeding
  • Surgical procedures, subclavian arterial puncture, trauma, and gastrointestinal or genitourinary bleeding within 14 days of the event
  • Patients taking oral anticoagulants and having an INR >1.7
  • A platelet count <100 000, venous glucose either <50 or >450
  • Premorbid mRS > 3

Treatment and study plan

Primary outcomes

  1. sICH

    Time frame: 72hours

    symptomatic ICH according to ECASS3

Secondary outcomes

  1. mRS 90 days

    Time frame: 90 days

    mRS 90 days

Sponsors and collaborators

Lead sponsor

University Hospital Tuebingen

Other

Collaborators

  • St John of God Hospital, Vienna

Registry information

Official study title

Thrombolysis in stRoke With Unknown onSet Based on Non-contrasT CT (TRUST CT). An International, Multicenter, Registry-based Study

Acronym: TRUST CT

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Aug 16, 2018
Registry last updated
Feb 4, 2019

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.

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