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Completed

NCT Number: NCT00279149

TRUST-tPA: Therapeutic Trial Evaluating Efficacy of Telemedicine (TELESTROKE) of Patients With Acute Stroke

The objective is to evaluate decision making of i.v. tPA treatment in acute stroke within 3 hours of symptom onset either remotely via videoconferencing system (investigational arm) beginning of treatment on-site and then transfer to stroke unit vs. decision after immediate transfer to stroke unit (usual care arm). Ten remote hospitals are connected to the BICHAT stroke unit. All patients will have stroke unit care at BICHAT hospital. Primary end-point is rankin 0-1 at 3 months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Hôpital d'Argenteuil, Emergency Unit, Argenteuil, France

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About this study

This study is a therapeutic trial, comparing a TELESTROKE decision making as the tested hypothesis to usual care (immediate transfer to stroke unit). Once the ER doctor in one of the 10 remote hospitals will judge his patient eligible for tPA thrombolysis, he will call the BICHAT stroke unit visio-conference system. Then, according to the randomization list, the patient will be allocated to 'standard care arm' which is the EMEA-approved tPA labeling (i.e., transfer the patient immediately to a stroke unit to have tPA thrombolysis if the patient arrives in due time -before 3 hours of stroke onset) or he will be allocated to 'TELESTROKE ARM"(i.e., remote neurological exam to perform NIHSS, assess the exact time of the first stroke symptoms onset and visualization of brain CT-scan by the vascular neurologist; then start the tPA thrombolysis on site if the indication is confirmed by the vascular neurologist, then transfer the patient to the BICHAT stroke unit). The primary outcome will be Rankin 0-1 (i.e., cured) at 3 months; secondary outcome will be death or dependency at 3 months and the frequency of symptomatic intracranial hemorrhage at 10 days. Patients randomized will be systematically transfer to the BICHAT stroke unit, no matter the received or not tPA thrombolysis, and no matter the study arm, according to the intention-to-treat rule.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patients older than 18 years
  • symptoms of brain infarction since less than 150 minutes
  • NIHSS between 4 and 22
  • No brain hemorrhage on contrast CT-scan
  • Signed consent form by the patient or his relatives

Exclusion criteria

  • NIHSS above 22 or coma
  • current oral anticoagulant or INR > 1.7
  • heparin treatment within the preceding 24 hours or prolonged APTT (>40seconds)
  • platelets count < 100 000/mm3
  • another stroke or brain trauma within 3 months prior admission
  • systolic blood pressure > 185 or diastolic blood pressure > 110 at the time od tPA treatment onset
  • neurologic deficit is improving
  • history of intracranial hemorrhage
  • glycemia less than 0.5g/l or upper than 4g/l after treatment by Actrapid
  • epileptic seizure at the time of stroke onset
  • Gastro-intestinal or urinary hemorrhage
  • Recent myocardial infarction within the last 21 days
  • Lumbar puncture or arterial blood sampling in a non compressible vessel within the last 7 days
  • Hemophilia
  • Pregnancy or breast feeding
  • Pericarditis within the last 3 months
  • Major surgery within the last 15 days
  • History of aortic dissection
  • Endocarditis with the last 3 months

Brain CT scan exclusion criteria:

  • Mass effect ( tumor, VAM, aneurism )
  • Decreased density ( ASPECTS score < 8) or mass effect involving more than 1/3 of the territory of the middle cerebral artery

Treatment and study plan

Visio conference system connected to the Tele-stroke network

Procedure

Visio conference system connected to the Tele-stroke network

Primary outcomes

  1. Percentage of patients cured at 3 months (rankin score 0,1)

    Time frame: at 3 months

    Percentage of patients cured at 3 months (rankin score 0,1)

Secondary outcomes

  1. NIHSS, rankin score ( 0,1,2) and Barthel Index at 3 months ,

    Time frame: at 3 months

    NIHSS, rankin score ( 0,1,2) and Barthel Index at 3 months ,

  2. percentage of symptomatic intracranial hemorrhage at 8 days

    Time frame: at 8 days

    percentage of symptomatic intracranial hemorrhage at 8 days

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Therapeutic Trial Evaluating Efficacy of Telemedicine (TELESTROKE) in the Management of Patient With Acute Stroke Within 3-hour After Their Symptom Onset Who Are Admitted to a Remote Hospital With no Stroke Unit Facility

Important dates

Study start
2006
Primary completion
2010
Study completion
2010
First posted
Jan 19, 2006
Registry last updated
Feb 17, 2011

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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