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Fructose for Acute Ischemic Stroke (FRUCTOSE-AIS)

2026. június 17. frissítette: Ji Xunming,MD,PhD

Clinical Study of Fructose Injection in the Treatment of Acute Ischemic Stroke

This is a single-center, prospective, randomized, open-label, blinded-endpoint exploratory clinical study enrolling 46 patients with acute ischemic stroke. All eligible patients have symptom onset within 4.5 hours, meet intravenous thrombolysis indications, and receive standard thrombolysis and routine stroke treatment. Participants are randomly assigned to two groups: the intervention group receives early intravenous infusion of 10% fructose injection plus standard treatment, while the control group receives only standard treatment without fructose. The study mainly evaluates changes in neurological function via NIHSS scores within 7 days after thrombolysis, assesses cerebral infarct lesion volume and brain edema using multimodal MRI including DWI, T2WI and MRS, detects cerebral neuronal metabolic markers, and conducts 1-month follow-up of neurological function by NIHSS score as well as functional prognosis using the mRS score. The research also comprehensively monitors adverse events and safety indicators to explore the clinical efficacy, neuronal metabolic regulation effect and safety of early fructose injection combined with intravenous thrombolysis in acute ischemic stroke patients, aiming to provide clinical evidence for early neuroprotective intervention.

A tanulmány áttekintése

Állapot

Aktív, nem toborzó

Körülmények

Beavatkozás / kezelés

Részletes leírás

This is an investigator-initiated, single-center, prospective, randomized, open-label, blinded-endpoint (PROBE) exploratory clinical trial. A total of 46 eligible patients with acute ischemic stroke within 4.5 hours of onset who meet the indications for intravenous thrombolysis will be enrolled. Participants are randomly assigned to an intervention group and a control group.The intervention group receives early intravenous infusion of 250 mL 10% fructose injection combined with standard intravenous thrombolysis and routine stroke background treatment. The control group receives only standard intravenous thrombolysis and conventional medical therapy without fructose intervention. All patients undergo standardized blood pressure and blood glucose management, and antiplatelet therapy is initiated 24 hours after thrombolysis.Neurological function is repeatedly assessed using the National Institutes of Health Stroke Scale (NIHSS) every 12 hours within 72 hours after thrombolysis and daily thereafter. Multimodal brain magnetic resonance examinations including DWI, T2WI and MRS are performed to evaluate cerebral infarct lesion volume, cerebral edema, and neuronal metabolic biomarkers such as NAA, Cho and Lac. The primary outcome is the change in NIHSS score at 7 days after thrombolysis, and cerebral neuronal metabolic characteristics. Secondary outcomes include dynamic neurological recovery, imaging changes of ischemic lesions, 1-month NIHSS score, 1-month modified Rankin Scale (mRS) functional prognosis.Prespecified subgroup analyses are conducted according to baseline neurological deficit severity, age, hypertension history and gender. Safety outcomes monitor adverse events such as hemorrhagic transformation, allergic reactions, liver and renal function abnormalities, blood glucose and electrolyte disorders to evaluate the clinical safety and tolerability of early fructose combined with thrombolysis.An independent clinical endpoint adjudication committee blindly assesses all endpoint events to reduce evaluation bias. Statistical analyses adopt appropriate methods for non-equilibrium small sample data to explore the clinical efficacy, neuronal mitochondrial metabolic regulation mechanism and safety of early fructose injection intervention in acute ischemic stroke patients, so as to provide clinical evidence for early neuroprotective strategy optimization.

Tanulmány típusa

Beavatkozó

Beiratkozás (Tényleges)

46

Fázis

  • 2. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi helyek

    • Jiangsu
      • Xuzhou, Jiangsu, Kína, 221000
        • Xuzhou Medical University Affiliated Hospital

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

  • Felnőtt
  • Idősebb felnőtt

Egészséges önkénteseket fogad

Nem

Leírás

Inclusion Criteria:

  1. Aged between 18 and 85 years, male and female are both eligible.
  2. Clinical diagnosis of acute ischemic stroke meeting the diagnostic criteria of Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke.
  3. Time from stroke onset to hospital admission ≤ 4.5 hours, with new ischemic lesions confirmed by emergency multimodal cranial MRI (DWI/T2WI).
  4. Meeting the indications for intravenous thrombolysis, without absolute contraindications to thrombolysis, and planned to receive standard intravenous thrombolysis.
  5. Relatively stable vital signs, able to complete baseline and follow-up cranial MRI examinations including DWI, T2WI and ¹H-MRS, as well as NIHSS and mRS scale assessments.
  6. The patient or legal representative voluntarily participates in the study and signs written informed consent.

Exclusion Criteria:

  1. History of fructose intolerance, abnormal fructose metabolism or hereditary fructose metabolic disorders.
  2. History of diabetes mellitus or random blood glucose > 11.1 mmol/L.
  3. Evidence of intracranial hemorrhage on CT scan, symptomatic intracranial hemorrhage, or clinical suspicion of subarachnoid hemorrhage.
  4. Requiring or intending to continue using restricted medications that may interfere with study safety and implementation.
  5. Unable to complete cranial MRI examination due to implanted metal materials, claustrophobia or other reasons.
  6. Any other conditions judged by the investigator to be inappropriate for enrollment.
  7. Presence of hemorrhagic diathesis, including but not limited to:

    • Known hereditary bleeding tendency or severe bleeding disease within the past 6 months;
    • Received heparin within 48 hours before enrollment with aPTT exceeding the upper limit of laboratory reference range;
    • Current use of vitamin K-dependent oral anticoagulants with INR > 1.7 or PT > 15 s, or current use of novel oral anticoagulants with prolonged aPTT/PT above laboratory upper limit;
    • Platelet count < 100,000/mm³ at screening;
    • History of central nervous system diseases such as tumor, aneurysm, intracranial or spinal surgery;
    • Received traumatic closed-chest cardiac massage, obstetric delivery or non-compressible vascular puncture within the past 10 days;
    • Suspected intracranial hemorrhage or aneurysmal subarachnoid hemorrhage;
    • Tumors with increased bleeding risk;
    • Peptic ulcer disease, esophageal varices, aneurysm, arterial/venous malformation within the past 3 months;
    • Any other known diseases associated with significantly elevated bleeding risk.
  8. Pre-stroke mRS score ≥ 2, combined with dementia or other neurological disabling diseases.
  9. Complicated with severe medical history affecting endpoint evaluation and follow-up, such as craniocerebral trauma, multiple sclerosis, encephalitis, tumor, poisoning, syphilis, or severe cardiac, pulmonary, hepatic, renal and endocrine diseases.
  10. Pregnant females.
  11. Currently participating in another investigational drug or device study, or participation in other experimental treatment within less than 30 days prior to enrollment.
  12. Combined with severe hepatic and renal insufficiency (eGFR < 30 mL/min/1.73m²).
  13. Refusal to sign informed consent.

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Kezelés
  • Kiosztás: Véletlenszerűsített
  • Beavatkozó modell: Párhuzamos hozzárendelés
  • Maszkolás: Egyetlen

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: Fructose Injection plus Standard Thrombolysis Treatment
Patients receive early intravenous infusion of 250 mL 10% fructose injection immediately after admission, followed by standard intravenous thrombolysis and routine standardized medical treatment for acute ischemic stroke. Unified blood pressure and blood glucose management are performed in all participants, and antiplatelet therapy is initiated 24 hours after thrombolysis.
Single intravenous infusion of 250 mL 10% fructose injection administered as early as possible within the ischemic stage, combined with standard intravenous thrombolysis and standardized basic treatment for acute ischemic stroke. Unified blood pressure and blood glucose management are implemented, and antiplatelet therapy is started 24 hours after thrombolysis.
Nincs beavatkozás: Standard Thrombolysis Alone Without Fructose
Patients receive only standard intravenous thrombolysis and routine standardized medical treatment for acute ischemic stroke without additional fructose injection. All participants receive the same unified blood pressure, blood glucose control and antiplatelet therapy regimen as the intervention group.

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
7-day change in National Institutes of Health Stroke Scale (NIHSS) score
Időkeret: Baseline to 7 days after thrombolysis
Absolute change in NIHSS score, calculated as follow-up score minus pre-intravenous thrombolysis (pre-IVT) baseline score, assessed at 7 days after intravenous thrombolysis (IVT). The full scale is the National Institutes of Health Stroke Scale; total score ranges from 0 to 42, and higher scores indicate more severe neurological deficits.
Baseline to 7 days after thrombolysis

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Levels of N-acetylaspartate (NAA) detected by proton magnetic resonance spectroscopy (¹H-MRS)
Időkeret: Pre-IVT baseline to 24 hours post-IVT (±2 hours)

Absolute changes in the levels of N-acetylaspartate (NAA) in the ischemic penumbra and infarct core, calculated from pre-IVT baseline to 24 hours after IVT. Relative quantification; no absolute concentration determined. Metabolite signal intensities are reported in arbitrary units (a.u.) normalized to internal reference (e.g., total NAA or water signal).

Unit of measure: Arbitrary units

Pre-IVT baseline to 24 hours post-IVT (±2 hours)
Levels of choline (Cho) detected by proton magnetic resonance spectroscopy (¹H-MRS)
Időkeret: Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours)

Absolute changes in the levels of choline (Cho) in the ischemic penumbra and infarct core, calculated from pre-IVT baseline to 24 hours after IVT. Relative quantification; no absolute concentration determined. Metabolite signal intensities are reported in arbitrary units (a.u.) normalized to internal reference (e.g., total Cho or water signal).

Unit of measure: Arbitrary units

Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours)
Levels of creatine (Cr) detected by proton magnetic resonance spectroscopy (¹H-MRS)
Időkeret: Pre-IVT baseline to 24 hours post-IVT (±2 hours)

Absolute changes in the levels of creatine (Cr) in the ischemic penumbra and infarct core, calculated from pre-IVT baseline to 24 hours after IVT. Relative quantification; no absolute concentration determined. Metabolite signal intensities are reported in arbitrary units (a.u.) normalized to internal reference (e.g., total Cr or water signal).

Arbitrary units

Pre-IVT baseline to 24 hours post-IVT (±2 hours)
NAA/Cr ratio derived from ¹H-MRS
Időkeret: Pre-IVT baseline to 24 hours post-IVT (±2 hours)

Absolute change in N-acetylaspartate/creatine (NAA/Cr) ratio in the ischemic penumbra and infarct core, calculated from pre-IVT baseline to 24 hours after IVT.

Unit of measure: Ratio (no unit)

Pre-IVT baseline to 24 hours post-IVT (±2 hours)
Cho/Cr ratio derived from ¹H-MRS
Időkeret: Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours)

Absolute change in choline/creatine (Cho/Cr) ratio in the ischemic penumbra and infarct core, calculated from pre-IVT baseline to 24 hours after IVT.

Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours). Unit of measure: Ratio (no unit)

Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours)
1-month change in National Institutes of Health Stroke Scale (NIHSS) score
Időkeret: Pre-IVT baseline to 1 month post-IVT (±7 days)
Absolute change in NIHSS score, calculated as follow-up score minus pre-IVT baseline score, assessed at 1 month after IVT. The full scale is the National Institutes of Health Stroke Scale; total score ranges from 0 to 42, and higher scores indicate more severe neurological deficits.
Pre-IVT baseline to 1 month post-IVT (±7 days)
1-month functional outcome assessed by modified Rankin Scale (mRS)
Időkeret: Pre-IVT baseline to 1 month post-IVT (±7 days)
Description: Functional status classified into favorable and unfavorable outcomes at 1 month after IVT. Favorable outcome: mRS score 0-2 (no or mild disability, independent in activities of daily living). Unfavorable outcome: mRS score 3-6 (moderate to severe disability, dependent in activities of daily living, or death for mRS score 6). The full scale is the modified Rankin Scale; total score ranges from 0 to 6, and higher scores indicate greater functional disability.
Pre-IVT baseline to 1 month post-IVT (±7 days)

Együttműködők és nyomozók

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Publikációk és hasznos linkek

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Általános kiadványok

Hasznos linkek

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete (Tényleges)

2026. június 5.

Elsődleges befejezés (Becsült)

2026. augusztus 1.

A tanulmány befejezése (Becsült)

2026. augusztus 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2026. május 23.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2026. június 2.

Első közzététel (Tényleges)

2026. június 4.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Tényleges)

2026. június 18.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2026. június 17.

Utolsó ellenőrzés

2026. június 1.

Több információ

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IPD terv leírása

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