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Acute Ischemic StrokeNCT07316049

Construction and Evaluation of an Intelligent Decision System for Reperfusion Therapy in Acute Ischemic Stroke

A study testing LingBao System in people with Acute Ischemic Stroke, run by Second Affiliated Hospital, Zhejiang University, School of Medicine.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

This multicenter, cluster-randomized controlled trial will evaluate the effectiveness and safety of the LingBao System, an AI-enabled clinical decision support platform for reperfusion therapy in acute ischemic stroke (AIS). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Ischemic Stroke
What is being tested?
LingBao System
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
3,000 participants
Where
No sites listed yet
Study dates
15 Jun 2026to 28 Feb 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years.
  • Clinical diagnosis of acute ischemic stroke (AIS).
  • Presentation within 24 hours of symptom onset or last-known-well.
  • Evaluated for reperfusion therapy (intravenous thrombolysis and/or endovascular treatment).

Who cannot join

  • Absence of key clinical or imaging data necessary for analysis.
  • Patients not undergoing reperfusion assessment or outside the pre-defined workflow.
  • Prior participation in other AI-based decision support trials within the past 12 months.
  • Explicit refusal of data use or withdrawal of consent (if applicable).

About this study

This multicenter, cluster-randomized controlled trial will evaluate the effectiveness and safety of the LingBao System, an AI-enabled clinical decision support platform for reperfusion therapy in acute ischemic stroke (AIS). Twenty certified stroke centers will be randomized 1:1 to LingBao-assisted care or standard care. Consecutive patients aged 18 years or older who present within 24 hours of symptom onset or last-known-well and are evaluated for intravenous thrombolysis and/or endovascular therapy will be prospectively enrolled.

The study initially plans to enroll approximately 3,000 patients from about 20 certified stroke centers, with approximately 150 patients per center. Because this is a cluster-randomized trial, a pre-specified blinded sample size re-estimation will be performed after approximately 40% of participants have completed the 90-day mRS assessment. The re-estimation will be based only on pooled, blinded information, including cluster size, cluster-size variability, intracluster correlation, follow-up completeness, missingness of the primary outcome, and the overall distribution of the 90-day mRS. No between-group treatment effect will be examined, and any sample size adjustment will only allow an increase in enrollment.

Read more

At intervention sites, clinicians may use the LingBao System during their routine workflows. The platform integrates routinely available clinical and imaging data, automatically estimates onset-to-treatment windows, screens contraindications, and provides evidence-based, guideline-concordant recommendations for reperfusion therapy; all treatment decisions remain at physician discretion.

The primary endpoint is the 90-day modified Rankin Scale (mRS) score analyzed by ordinal shift. Secondary endpoints include workflow metrics (door-to-needle time and door-to-puncture time), reperfusion treatment rates, early neurological improvement, symptomatic intracranial hemorrhage, and mortality.

The findings will provide real-world evidence on the clinical value of AI-assisted decision support for reperfusion therapy in AIS and inform broader implementation of intelligent stroke management systems.

Read the detailed description

The LingBao System (Stroke Reperfusion Intelligent Decision System, SRIDS) is an AI-based clinical decision support platform designed to assist physicians in the evaluation and treatment decision-making process for acute ischemic stroke (AIS) patients eligible for reperfusion therapy. Built upon the 2024 Chinese Guidelines for Reperfusion Therapy in Acute Ischemic Stroke, major international randomized controlled trial (RCT) evidence, and large-scale real-world datasets, LingBao integrates clinical information, imaging parameters, and guideline-based criteria to provide transparent, evidence-graded recommendations for intravenous thrombolysis and/or endovascular therapy.

This multicenter, cluster-randomized controlled trial aims to assess the real-world effectiveness and safety of LingBao in optimizing reperfusion decision-making and improving patient outcomes. Twenty certified stroke centers in China will be randomized 1:1 to either LingBao-assisted care or standard care. Consecutive adult patients (≥18 years) presenting within 24 hours of last-known-well and evaluated for reperfusion therapy will be prospectively enrolled.

The initial target sample size is approximately 3,000 participants enrolled from about 20 certified stroke centers randomized in a 1:1 ratio. This target accounts for the cluster-randomized design and the anticipated intracluster correlation. To preserve adequate statistical power in the presence of uncertainty regarding the intracluster correlation, unequal cluster sizes, follow-up completion, and the overall distribution of the 90-day modified Rankin Scale, the protocol includes a pre-specified blinded sample size re-estimation. The blinded re-estimation will be conducted once approximately 40% of participants have completed the 90-day primary outcome assessment. An independent statistician will perform this analysis using pooled data without access to treatment allocation. The re-estimation will not include any between-group comparison or treatment-effect estimate. Parameters considered will include the actual mean cluster size, variability in cluster size, intracluster correlation, 90-day follow-up completion, missingness of the primary outcome, and the overall mRS distribution. If the updated design effect or other blinded assumptions indicate that the current sample size may provide insufficient statistical power, enrollment may be increased. Any adjustment will be limited to an increase in sample size and will be implemented by extending recruitment at existing centers or, if necessary, adding additional certified stroke centers. The procedure is designed to maintain the integrity of randomization and control the type I error rate.

At intervention sites, clinicians may use LingBao during standard clinical workflows. The system automatically calculates the estimated onset-to-treatment window, screens contraindications, summarizes imaging-based eligibility criteria, and displays guideline-concordant recommendations along with their class and level of evidence. LingBao does not replace physician judgment; all clinical decisions remain entirely at the discretion of the treating team.

Data on patient demographics, baseline characteristics, workflow times, treatments, and outcomes will be collected through standardized electronic case report forms (eCRFs). The primary outcome is functional status at 90 days, measured by the modified Rankin Scale (mRS) and analyzed using an ordinal shift model. Key secondary outcomes include door-to-needle time (DNT) for intravenous thrombolysis, door-to-puncture time (DPT) for endovascular therapy, rates of reperfusion treatment, early neurological improvement, symptomatic intracranial hemorrhage, and mortality.

By systematically integrating AI-driven clinical reasoning with evidence-based medicine, the LingBao study aims to establish an intelligent, reproducible, and guideline-concordant framework for acute stroke management. The results are expected to inform large-scale implementation of AI-supported decision systems to enhance the quality, consistency, and efficiency of stroke reperfusion therapy in real-world practice.

Being tested
LingBao System, Standard Care
Keywords
Reperfusion Therapy, Artificial Intelligence, Clinical Decision Support System
Medical subject headings
Ischemic Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LingBao SystemOther

    Also called LingBao AI Decision Platform; SRIDS; Intelligent Stroke Reperfusion Decision Support System

    The LingBao System is an artificial intelligence-enabled clinical decision support platform developed to assist physicians in evaluating and managing patients with acute ischemic stroke (AIS) who are candidates for reperfusion therapy.

    The system integrates routinely available clinical and imaging data, automatically estimates onset-to-treatment windows, screens contraindications, and displays guideline-concordant recommendations for intravenous thrombolysis and/or endovascular therapy along with corresponding evidence levels.

    LingBao is intended for use by trained clinicians as an informational tool within standard care pathways. It does not replace physician judgment, modify treatment protocols, or deliver any direct therapeutic intervention.

    LingBao will be available only at centers randomized to the intervention arm ("LingBao-Assisted Care"). Clinicians at control centers ("Standard Care") will not use the system during the study period.

  • Standard CareOther

    Participants at stroke centers assigned to the Standard Care arm will receive routine clinical management for acute ischemic stroke (AIS) according to current national and international guidelines.

Study groups in NCT07316049
Study groupRoleWhat they receive
LingBao-Assisted CareExperimentalParticipants enrolled at stroke centers assigned to the LingBao-assisted group will receive routine clinical care for acute ischemic stroke, with optional use of the LingBao System (Stroke Reperfusion Intelligent Decision System, SRIDS) as a clinical decision support tool during evaluation and management for reperfusion therapy. The LingBao System integrates patient demographic, clinical, and imaging data; automatically estimates onset-to-treatment windows; screens contraindications; and provides guideline-concordant recommendations for intravenous thrombolysis and/or endovascular therapy with evidence grading. All final treatment decisions remain at the discretion of the treating physicians.
Receives: Other: LingBao System
Standard CareActive comparatorParticipants enrolled at stroke centers assigned to the control group will receive standard care for acute ischemic stroke according to current national and international guidelines. Clinicians in these centers will not access or use the LingBao System during the study period. All diagnostic and therapeutic decisions will follow usual institutional practice without AI-based support.
Receives: Other: Standard Care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Functional outcome at 90 days assessed by the modified Rankin Scale (mRS)

    Functional status at 90 days after stroke onset will be measured using the modified Rankin Scale (mRS, range 0-6). Outcomes will be analyzed as an ordinal shift across the full mRS distribution, comparing LingBao-assisted care versus standard care.

    Measured: 90 days post-stroke onset

Secondary outcomes (5)
  1. Door-to-Needle Time (DNT) for Intravenous Thrombolysis at baseline

    Time interval between hospital arrival and initiation of intravenous thrombolysis among patients receiving IVT.

    Measured: Baseline

  2. Door-to-Puncture Time (DPT) for Endovascular Therapy at baseline

    Time interval between hospital arrival and arterial puncture for patients undergoing endovascular therapy.

    Measured: Baseline

  3. Reperfusion Treatment Rate at baseline

    Proportion of eligible acute ischemic stroke patients who received intravenous thrombolysis and/or endovascular therapy.

    Measured: Baseline

  4. Symptomatic Intracranial Hemorrhage (sICH) within 36 hours after treatment

    Occurrence of symptomatic intracranial hemorrhage within 36 hours after reperfusion therapy, defined according to ECASS III criteria.

    Measured: Within 36 hours after treatment

  5. All-Cause Mortality at 90 days post-stroke onset

    All-cause mortality within 90 days after stroke onset.

    Measured: 90 days post-stroke onset

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jan 2026
  2. Study start15 Jun 2026 (estimated)
  3. Primary completion31 Oct 2026 (estimated)
  4. Study completion28 Feb 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
Twenty certified stroke centers will be randomized 1:1 to LingBao-assisted care or standard care.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
3,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07316049
Sponsor's protocol ID
LingBao
Status last verified
Oct 2025
First submitted
2 Dec 2025
Last updated
4 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing LingBao System in people with Acute Ischemic Stroke, run by Second Affiliated Hospital, Zhejiang University, School of Medicine.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 4 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Functional outcome at 90 days assessed by the modified Rankin Scale (mRS) (time frame: 90 days post-stroke onset). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Jun 2026.

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