Fructose for Acute Ischemic Stroke (FRUCTOSE-AIS)
Clinical Study of Fructose Injection in the Treatment of Acute Ischemic Stroke
調査の概要
詳細な説明
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
研究場所
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Jiangsu
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Xuzhou、Jiangsu、中国、221000
- Xuzhou Medical University Affiliated Hospital
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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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介入なし: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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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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7-day change in National Institutes of Health Stroke Scale (NIHSS) score
時間枠: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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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Levels of N-acetylaspartate (NAA) detected by proton magnetic resonance spectroscopy (¹H-MRS)
時間枠:Pre-IVT baseline to 24 hours post-IVT (±2 hours)
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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)
時間枠: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)
時間枠:Pre-IVT baseline to 24 hours post-IVT (±2 hours)
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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
時間枠: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
時間枠:Time Frame: Pre-IVT baseline to 24 hours post-IVT (±2 hours)
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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
時間枠: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)
時間枠: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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協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
- 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.
便利なリンク
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- AIS-FRUCTOSE
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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