Upfront Lipid-Lowering Therapy With Statins Combined With Hybutimibe in Patients With Acute Ischemic Stroke or Transient Ischemic Attack.
This study aims to evaluate whether an upfront combination lipid-lowering therapy (statins combined with hybutimibe) can further improve the 8-week LDL-C target achievement rate (<1.8 mmol/L and ≥50% reduction from baseline) compared with a sequential lipid-lowering therapy in patients with acute ischemic stroke or transient ischemic attack (TIA)
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ 3
連絡先と場所
研究連絡先
研究連絡先
- 名前:Zhiyuan Feng
- 電話番号:86-010-59975672
- メール:fzyhhz1996@gmail.com
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Definite diagnosis of acute ischemic stroke or TIA.
- Age ≥18 and <75 years
- Time from onset (last known normal) to enrollment ≤ 72 hours.
- LDL-C level ≥ 1.8 mmol/L prior to enrollment (must obtain LDL-C value after onset to be randomized).
Exclusion Criteria:
-
Use of high-intensity statins, cholesterol absorption inhibitors, PCSK9 inhibitors, or other small interfering RNA cholesterol-lowering drugs within 14 days prior to randomization.
-
Suspected familial hypercholesterolemia.
-
Suspected cardiogenic stroke (e.g., with atrial fibrillation, prosthetic heart valves, atrial myxoma, endocarditis).
-
Acute ischemic stroke suspected to be caused by other etiologies (e.g., arterial dissection, vasculitis, vascular malformation).
-
Presence of isolated sensory symptoms (e.g., numbness) only, isolated visual changes only, or isolated dizziness/vertigo only, in the absence of evidence of acute infarction on baseline head CT or MRI.
-
Pre-stroke mRS score >2.
-
High risk of cerebral hemorrhage (e.g., imaging indicates hemorrhagic transformation after the current stroke, or history of hemorrhagic stroke).
-
Patients with risks or contraindications to statins or hybutimibe:
- Acute liver failure or decompensated cirrhosis.
- Known hypersensitivity to statins or hybutimibe.
- Pregnant or breastfeeding women, or women of childbearing potential who are not using effective contraceptive measures and have no documented pregnancy test.
- Use of immunosuppressants, azole antifungals, amiodarone, fibrates, or other medications that may affect statin metabolism within 14 days prior to randomization, or planned use of such medications during the study period.
- Hepatic or renal impairment (hepatic impairment defined as ALT >2× upper limit of normal [ULN] or AST >2× ULN; renal impairment defined as serum creatinine >1.5× ULN or estimated glomerular filtration rate [eGFR] <20 mL/min).
- Creatine kinase >5× ULN, or a personal or family history of hereditary muscle disease.
-
Planned major surgery or interventional procedure within 8 weeks that may require interruption of the study drug.
-
Severe organic disease with a life expectancy < 8 weeks.
-
Currently participating in other investigational drug or device studies.
-
Inability to complete the 8-week follow-up due to geographic or other reasons (e.g., dementia, severe paralysis, psychiatric disorders).
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
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:Upfront combination Lipid Lowering Therapy
Patients will receive a combination of Atorvastatin (40 mg/day) and Hybutimibe (10 mg/day) immediately after enrollment, continuing for 8 weeks |
40 mg/day, administered orally 10 mg/day, administered orally. Used upfront in the experimental group, and sequentially added in the active comparator group if the 4-week LDL-C target is not met. |
|
アクティブコンパレータ:Sequential Lipid Lowering Therapy
Patients will receive Atorvastatin (40 mg/day) immediately after enrollment for 4 weeks. An LDL-C test will be performed at 4 weeks; if the target is achieved (<1.8 mmol/L and ≥50% reduction from baseline), the same regimen will continue until 8 weeks. If the target is not achieved, Hybutimibe (10 mg/day) will be added to the regimen until 8 weeks |
40 mg/day, administered orally 10 mg/day, administered orally. Used upfront in the experimental group, and sequentially added in the active comparator group if the 4-week LDL-C target is not met. |
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Percentage of patients achieving the LDL-C target at 8 weeks
時間枠:at 8 weeks
|
Defined as achieving an LDL-C level of <1.8 mmol/L and a reduction of ≥50% from baseline |
at 8 weeks
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Percentage change in the lipid profile at 8 weeks
時間枠:at 8 weeks
|
Evaluated by the least squares mean percentage change from baseline in LDL-C, non-HDL-C, TG, TC, Lp(a), and ApoB. |
at 8 weeks
|
|
Percentage of patients achieving the general LDL-C target at 8 weeks
時間枠:at 8 weeks
|
Defined as achieving an LDL-C level of <1.8 mmol/L at 8 weeks |
at 8 weeks
|
|
Incidence of composite vascular events at 8 weeks
時間枠:at 8 weeks
|
Including stroke (ischemic or hemorrhagic stroke), myocardial infarction, and cardiovascular death. |
at 8 weeks
|
|
All-cause mortality rate at 8 weeks
時間枠:at 8 weeks
|
Incidence of death from any cause during the study period |
at 8 weeks
|
|
Stroke recurrence rate at 8 weeks
時間枠:at 8 weeks
|
Incidence of recurrent stroke events during the follow-up period |
at 8 weeks
|
|
Percentage of patients with a favorable functional outcome at 8 weeks
時間枠:at 8 weeks
|
Defined as a modified Rankin Scale (mRS) score of 0 to 2 |
at 8 weeks
|
|
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 up to 8 weeks
時間枠:Up to 8 weeks
|
Defined as the occurrence of any of the following prespecified safety events: study drug discontinuation or dose reduction due to intolerance, newly diagnosed diabetes, muscle-related adverse events (myalgia, myopathy, muscle necrosis), elevated liver enzymes (ALT or AST > 3 times the upper limit of normal), or major bleeding events. |
Up to 8 weeks
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- 20260528-Hybutimibe
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?
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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