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Completed

NCT Number: NCT02854592

Intravenous Thrombolysis Registry for Chinese Ischemic Stroke Within 4.5 h Onset

Stroke is one of the leading causes of death and disability in China. Intravenous thrombolysis with recombinant tissue plasminogen activator (rtPA) improves the outcome for ischemic stroke patients who can be treated within 4.5 hours of symptom onset. In China, in addition to rt-PA, intravenous urokinase within 6 h has also been recommended by the 2010 Chinese Guidelines for the Diagnosis and Treatment of Patients with Acute Ischemic Stroke, and supported by evidence from two intravenous urokinase thrombolysis trials. Urokinase is used more frequently than rt-PA, mainly because it is cheaper. To describe Chinese experience with thrombolytic therapy for Ischemic Stroke within 4.5h onset, we designed a multicenter, prospective, registry study. The aim of INtravenous Thrombolysis REgistry for Chinese Ischemic Stroke within 4.5 h onset(INTRECIS)was to assess the safety and efficacy of intravenous rtPA, urokinase as thrombolytic therapy within the first 4.5 h of onset of acute ischaemic stroke.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

General Hospital of ShenYang Military Region

Shenyang, China

About this study

INTRECIS is a prospective multicenter registry using data from 60 centres in the North China. Consecutive patients with acute ischemic stroke who are treated with intravenous rtPA, urokinase within 4.5 hours of symptom onset in 60 centres of the North China will be eligible for this registry. Patient involvement in the registry shall not influence any treatment decision. Patients will undergo a complete diagnostic work up including a clinical neurological examination using the National Institutes of Health Stroke Scale (NIHSS) score, laboratory examination, brain and neurovascular imaging, echocardiography, 24-hours ECG. Clinical outcome will be evaluated on day 1 and day 14 using the National Institute of Health Stroke Scale (NIHSS) score, evaluated at 3 months using modified Rankin Scale score (mRS) and assessing adverse events. The proportion of patients with excellent outcome (mRS 0 to 1) at 3 months after treatment will serve as the primary outcome. Secondary outcome measures will include independent functional outcome (mRS 0 to 2), changes in NIHSS at 1 and 14 day compared with baseline, symptomatic intracerebral haemorrhage, recurrent stroke and all-cause mortality.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • ischemic stroke diagnosed by CT or MRI
  • first stroke onset or past stroke without obvious neurological deficit (mRS≤1)
  • Time from onset to treatment: ≤ 4.5 hours
  • Treatment with intravenous rtPA or urokinase
  • Signed informed consent by patient self or legally authorized representatives

Exclusion criteria

  • History of subarachnoid hemorrhage, intracranial hemorrhage and hemorrhagic cerebral infarction
  • Obvious head injuries or strokes within 3 months
  • Intracranial tumor, arteriovenous malformation or aneurysm
  • Intracranial or spinal cord surgery within 3 months
  • Gastrointestinal or urinary tract hemorrhage within the previous 21 days
  • Blood glucose < 50 mg/dl (2.7mmol/L)
  • Heparin therapy or oral anticoagulation therapy within 48 hours
  • Oral warfarin is being taken and INR>1.6
  • Severe systemic disease which is expected to survive less than 3 months
  • Major surgery within 1 month
  • Uncontrolled hypertension (>180/100 mmHg)
  • Platelet count < 10×109/L
  • Patients who have been involved in other clinical trials within 3 months

Treatment and study plan

rtPA

Drug

intravenous thrombolysis with rtPa

Other names: alteplase

Urokinase

Drug

intravenous thrombolysis with urokinase

Primary outcomes

  1. Excellent outcome at 3 months

    Time frame: 90 days

    The proportion of patients with excellent outcome (modified Rankin Score 0 to 1) at 3 months after stroke onset

Secondary outcomes

  1. Functional independence at 3 months after stroke onset

    Time frame: 90 days

    the proportion of patients with functional independence (modified Rankin Scale, mRS, score 0-2) at 3 months after stroke onset

  2. Symptomatic intracerebral haemorrhage

    Time frame: 22-36 hours

    Symptomatic intracranial haemorrhages defined as NIHSS score increase ≥4 caused by intracranial hemorrhage

  3. Recurrent stroke

    Time frame: 90 days

    New stroke or TIA within 3 months

  4. All-cause mortality

    Time frame: 1 day, 14 days, 90 days

    Death from all-cause death, stroke events or cardiovascular events

  5. changes in NIHSS score

    Time frame: 1 day, 14 days

    changes in NIHSS score at 1 day and 14 days, compared with baseline

Sponsors and collaborators

Lead sponsor

General Hospital of Shenyang Military Region

Other

Registry information

Acronym: INTRECIS

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Aug 3, 2016
Registry last updated
Dec 17, 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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