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- Klinische proef NCT07908875
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)
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 3
Contacten en locaties
Studiecontact
- Naam: Zhiyuan Feng
- Telefoonnummer: 86-010-59975672
- E-mail: fzyhhz1996@gmail.com
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
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).
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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.
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Pre-stroke mRS score >2.
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High risk of cerebral hemorrhage (e.g., imaging indicates hemorrhagic transformation after the current stroke, or history of hemorrhagic stroke).
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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.
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Planned major surgery or interventional procedure within 8 weeks that may require interruption of the study drug.
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Severe organic disease with a life expectancy < 8 weeks.
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Currently participating in other investigational drug or device studies.
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Inability to complete the 8-week follow-up due to geographic or other reasons (e.g., dementia, severe paralysis, psychiatric disorders).
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 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. |
|
Actieve vergelijker: 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. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Percentage of patients achieving the LDL-C target at 8 weeks
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Percentage change in the lipid profile at 8 weeks
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: at 8 weeks
|
Including stroke (ischemic or hemorrhagic stroke), myocardial infarction, and cardiovascular death. |
at 8 weeks
|
|
All-cause mortality rate at 8 weeks
Tijdsspanne: at 8 weeks
|
Incidence of death from any cause during the study period |
at 8 weeks
|
|
Stroke recurrence rate at 8 weeks
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
|
Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Cerebrovasculaire aandoeningen
- Hersenziekten
- Ziekten van het centrale zenuwstelsel
- Ziekten van het zenuwstelsel
- Vaatziekten
- Hart-en vaatziekten
- Ischemie van de hersenen
- Hartinfarct
- Ischemische beroerte
- Ischemische aanval, voorbijgaand
- Heterocyclische verbindingen, 1-ring
- Heterocyclische verbindingen
- Vetzuren
- Lipiden
- Azoles
- Pyrroles
- Heptaanzuren
- Atorvastatine
Andere studie-ID-nummers
- 20260528-Hybutimibe
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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