- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07626541
Fructose for Acute Ischemic Stroke (FRUCTOSE-AIS)
Clinical Study of Fructose Injection in the Treatment of Acute Ischemic Stroke
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Réel)
Phase
- Phase 2
Contacts et emplacements
Lieux d'étude
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Jiangsu
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Xuzhou, Jiangsu, Chine, 221000
- Xuzhou Medical University Affiliated Hospital
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Aged between 18 and 85 years, male and female are both eligible.
- Clinical diagnosis of acute ischemic stroke meeting the diagnostic criteria of Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke.
- Time from stroke onset to hospital admission ≤ 4.5 hours, with new ischemic lesions confirmed by emergency multimodal cranial MRI (DWI/T2WI).
- Meeting the indications for intravenous thrombolysis, without absolute contraindications to thrombolysis, and planned to receive standard intravenous thrombolysis.
- 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.
- The patient or legal representative voluntarily participates in the study and signs written informed consent.
Exclusion Criteria:
- History of fructose intolerance, abnormal fructose metabolism or hereditary fructose metabolic disorders.
- History of diabetes mellitus or random blood glucose > 11.1 mmol/L.
- Evidence of intracranial hemorrhage on CT scan, symptomatic intracranial hemorrhage, or clinical suspicion of subarachnoid hemorrhage.
- Requiring or intending to continue using restricted medications that may interfere with study safety and implementation.
- Unable to complete cranial MRI examination due to implanted metal materials, claustrophobia or other reasons.
- Any other conditions judged by the investigator to be inappropriate for enrollment.
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.
- Pre-stroke mRS score ≥ 2, combined with dementia or other neurological disabling diseases.
- 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.
- Pregnant females.
- Currently participating in another investigational drug or device study, or participation in other experimental treatment within less than 30 days prior to enrollment.
- Combined with severe hepatic and renal insufficiency (eGFR < 30 mL/min/1.73m²).
- Refusal to sign informed consent.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: 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.
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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.
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Aucune intervention: 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.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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7-day change in National Institutes of Health Stroke Scale (NIHSS) score
Délai: Baseline to 7 days after thrombolysis
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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.
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Baseline to 7 days after thrombolysis
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Levels of N-acetylaspartate (NAA) detected by proton magnetic resonance spectroscopy (¹H-MRS)
Délai: 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)
|
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Levels of choline (Cho) detected by proton magnetic resonance spectroscopy (¹H-MRS)
Délai: Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours)
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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)
|
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Levels of creatine (Cr) detected by proton magnetic resonance spectroscopy (¹H-MRS)
Délai: 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)
|
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NAA/Cr ratio derived from ¹H-MRS
Délai: Pre-IVT baseline to 24 hours post-IVT (±2 hours)
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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)
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Cho/Cr ratio derived from ¹H-MRS
Délai: 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)
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1-month change in National Institutes of Health Stroke Scale (NIHSS) score
Délai: Pre-IVT baseline to 1 month post-IVT (±7 days)
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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.
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Pre-IVT baseline to 1 month post-IVT (±7 days)
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1-month functional outcome assessed by modified Rankin Scale (mRS)
Délai: Pre-IVT baseline to 1 month post-IVT (±7 days)
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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.
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Pre-IVT baseline to 1 month post-IVT (±7 days)
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Collaborateurs et enquêteurs
Parrainer
Publications et liens utiles
Publications générales
- Zhang D, Feng Y, Pan H, Xuan Z, Yan S, Mao Y, Xiao X, Huang X, Zhang H, Zhou F, Chen B, Chen X, Liu H, Yan X, Liang H, Cui W. 9-Methylfascaplysin exerts anti-ischemic stroke neuroprotective effects via the inhibition of neuroinflammation and oxidative stress in rats. Int Immunopharmacol. 2021 Aug;97:107656. doi: 10.1016/j.intimp.2021.107656. Epub 2021 Apr 23.
- Tian Y, Su Y, Ye Q, Chen L, Yuan F, Wang Z. Silencing of TXNIP Alleviated Oxidative Stress Injury by Regulating MAPK-Nrf2 Axis in Ischemic Stroke. Neurochem Res. 2020 Feb;45(2):428-436. doi: 10.1007/s11064-019-02933-y. Epub 2019 Dec 19.
- Marek G, Pannu V, Shanmugham P, Pancione B, Mascia D, Crosson S, Ishimoto T, Sautin YY. Adiponectin resistance and proinflammatory changes in the visceral adipose tissue induced by fructose consumption via ketohexokinase-dependent pathway. Diabetes. 2015 Feb;64(2):508-18. doi: 10.2337/db14-0411. Epub 2014 Sep 3.
- Kim YN, Jung HY, Eum WS, Kim DW, Shin MJ, Ahn EH, Kim SJ, Lee CH, Yong JI, Ryu EJ, Park J, Choi JH, Hwang IK, Choi SY. Neuroprotective effects of PEP-1-carbonyl reductase 1 against oxidative-stress-induced ischemic neuronal cell damage. Free Radic Biol Med. 2014 Apr;69:181-96. doi: 10.1016/j.freeradbiomed.2014.01.006. Epub 2014 Jan 17.
- Hayasaki T, Ishimoto T, Doke T, Hirayama A, Soga T, Furuhashi K, Kato N, Kosugi T, Tsuboi N, Lanaspa MA, Johnson RJ, Maruyama S, Kadomatsu K. Fructose increases the activity of sodium hydrogen exchanger in renal proximal tubules that is dependent on ketohexokinase. J Nutr Biochem. 2019 Sep;71:54-62. doi: 10.1016/j.jnutbio.2019.05.017. Epub 2019 Jun 8.
Liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- AIS-FRUCTOSE
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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