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Cohort Study for Severe Ischaemic Stroke

Clinical Features, Management and Outcomes of Severe Ischaemic Stroke in Tertiary Hospitals in China: a Multi-centre Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03222024
Acronym
SIS
Enrollment
2500
Registered
2017-07-19
Start date
2017-09-12
Completion date
2020-08-31
Last updated
2020-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe Ischaemic Stroke, Malignant Ischaemic Stroke

Keywords

ischaemic stroke, severe, malignant, courses, risk factors, clinical course, management, prognosis

Brief summary

This is a multi-centre, prospective cohort study. The aim of this study is to investigate causes, risk factors, clinical course, management and outcomes of severe ischaemic stroke in a real-world setting in tertiary hospitals in China. Patients with acute ischaemic stroke from nine tertiary hospitals in western China will be recruited. Participants will be visited within 24 hours after admission, on day 3, day 7 and at discharge, to collect their clinical data, blood biomarkers, and brain imaging. A structured telephone interview will be conducted for each participant at 3 months and 1 year after stroke onset, respectively, to collect their functional outcomes. In-hospital outcomes include haemorrhagic transformation, brain oedema and death, 3-month and 1-year outcomes include survival status (death or survival) and functional outcome (scores of modified Rankin scale, mRS).

Detailed description

Nine tertiary hospitals in Western China are participating in the study. In each participating hospital, stroke patients admitted to the Department of Neurology will be screened by their responsible doctors for eligibility. For patients who are potentially eligible, the doctor will introduce this study in detail with written information to the patient or their legal proxies. After participants (or their proxies) sign the consent form, investigators will collect their baseline data within 24 hours after admission (visit 1). Subsequent visits will be conducted on day 3 of admission or if the patient experiences neurological deterioration between visit 1 and day 3 (visit 2), on day 7 of admission or if neurological deterioration occurs between visit 2 and day 7 (visit 3), and on the day before discharge or on day 30 of admission, whichever is earlier (visit 4). At visit 1 investigators will record demographics, medical history, characteristics of current stroke, and results of the blood tests, brain imaging and other examinations, if applicable. At visit 4, investigators will record interventions and rehabilitation used during hospitalisation. At day 90 and 1 year of stroke onset, a trained investigator (neurologist) blind to all medical information will contact the participant to deliver a structured telephone interview and collect their functional outcomes. Objectives of this study are: a) to explore causes of clinical worsening in acute ischaemic stroke, and for each type of clinical worsening to dynamically evaluate its clinical course and explore its risk factors; b) to explore the application of conventional stroke therapies in patients with severe ischaemic stroke in China; c) to investigate factors precipitating and predisposing malignant brain oedema following acute ischaemic stroke; and d) to better select patients with malignant brain oedema for individualised treatment strategies.

Interventions

This is an observational study for clinical course and outcomes of severe ischaemic stroke; therefore, interventions are prescribed by responsible doctors based on patients' clinical conditions, which is not interfered by current study

Sponsors

Sichuan Academy of Medical Sciences
CollaboratorOTHER
The Affiliated Hospital Of Southwest Medical University
CollaboratorOTHER
Affiliated Hospital of North Sichuan Medical College
CollaboratorOTHER
Chengdu University of Traditional Chinese Medicine
CollaboratorOTHER
Mianyang Central Hospital
CollaboratorOTHER
People's Hospital of Deyang City
CollaboratorUNKNOWN
The First People's Hospital of Ziyang
CollaboratorUNKNOWN
Jiangyou People's Hospital
CollaboratorUNKNOWN
Science and Technology Department of Sichuan Province
CollaboratorOTHER
National Natural Science Foundation of China
CollaboratorOTHER_GOV
West China Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 years or over * Symptoms and signs of clinically definite acute stroke * Time of stroke onset is known and within 30 days of admission * CT or MRI brain scanning has reliably excluded both intracranial haemorrhage and structural brain lesions which can mimic stroke (e.g. brain tumour)

Exclusion criteria

* Likely to be unavailable for follow-up, e.g. no fixed home address * Refuse to give consent to participate

Design outcomes

Primary

MeasureTime frameDescription
Functional outcome at 3 months after stroke onset3 months after stroke onsetModified Rankin scale score of patients at 3 months after the onset of ischaemic stroke.

Secondary

MeasureTime frameDescription
Proportion of patients experiencing clinical worsening following acute ischaemic stroke30 days after admissionClinical worsening is defined as a) neurological deterioration with an increase of NIHSS score of 4 or more as compared to baseline NIHSS, b) a decline of consciousness, which leads to a GCS score of 8 or less, or item 1a of NIHSS scored 1 or over, c) need for invasive interventions such as hemicraniectomy, or d) death in hospital.
Proportion of patients with malignant brain oedema following acute ischaemic stroke30 days after admissionMalignant brain oedema is defined as symptoms or signs of clinical worsening associated with imaging evidence of space-occupying brain oedema.
Proportion of patients with initially severe ischaemic stroke24 hours after admissionInitially severe ischaemic stroke is defined as a) severe neurological deficits, assessed by the National Institute of Health Stroke Scale (NIHSS) scored 15 or over, b) loss of consciousness, assessed by the Glasgow Coma Scale (GCS) scored 8 or less, or item 1a of NIHSS scored 1 or over, or c) intubation, mechanical ventilation, or admitted to intensive care unit on admission.
Changes in consicousness level of patients with initially severe stroke from day 0, day 3, day 7 to day 30 after admission.30 days after admissionDynamically record scores of Glasgow Coma Scale (GCS)
Functional outcome at 1 year after stroke onset1 year after stroke onsetModified Rankin scale score of patients at 1 year after the onset of ischaemic stroke.
Clinical course of stroke severity in patients with initially severe stroke30 days after admissionDynamically record scores of National Institute of Health Stroke Scale (NIHSS) from day 0, day 3, day 7 to day 30 after admission.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026