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Completed

NCT Number: NCT05996978

Intensive Drug Therapy for Ischemic Stroke Caused by Severe Intracranial Arterial Stenosis

To observe the safety and efficacy of intensive drug therapy for ischemic stroke caused by severe intracranial arterial stenosis.Patients with acute stroke caused by intracranial arterial stenosis (stenosis rate ≥70%) were enrolled and accept dual antiplatelet therapy (DAPT) (aspirin 100 mg/d and clopidogrel 75 mg/d for 90 days, followed by aspirin 100 mg/d for long term) under the guidance of platelet function analysis (Verifynow) combined with the intensive statin therapy (40 mg/d for 14 days, followed by 20 mg/d for long term).

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Key information

Age range

35 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine

Shanghai, China

About this study

Patients (35 to 80 years ) with acute ischemic stroke, who can be treated within 72 hours of symptom onset will be enrolled. Patients fulfilling all of the inclusion criteria and none of the exclusion criteria will be randomly selected.Patients were treated with dual antiplatelet therapy (DAPT) (aspirin 100 mg per day and clopidogrel 75 mg per day were administered for 90 days, followed by aspirin 100 mg per day for long term) and atorvastatin (40 mg per day for 14 days, followed by 20 mg per day long term) after enrollment. Patients with aspirin resistance (aspirin reaction units [ARU] ≥550) or clopidogrel resistance (P2Y12 reaction units [PRU] ≥208) were excluded on the 7th day of therapy.The primary objective is to observe the safety and efficacy of intensive drug therapy for ischemic stroke patients. A Data and Safety Monitoring Board (DSMB) will regularly monitor safety during the study. The trial has been approved by Ethics Committee of Yueyang Hospital of Integrated Traditional Chinese and Western Medicine affiliated to Shanghai University of Traditional Chinese Medicine.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 35 and 80 years;
  • Onset <72 hours;
  • New-onset ischemic stroke confirmed by skull magnetic resonance diffusion weighted imaging (MR-DWI);
  • Severe ICAS (stenosis ≥70%) indicated by time-of-flight magnetic resonance angiography (TOF-MRA).

Exclusion criteria

  • Ischemic stroke caused by other etiological factors (e.g., cardio-embolism, arterial dissection, vasculitis, etc.);
  • Post-infarction hemorrhagic transformation and intraplaque hemorrhage as indicated by imaging examination;
  • Contraindications to aspirin, clopidogrel, or atorvastatin;
  • Intracranial hemorrhage within 3 months and a recent history of surgery or trauma;
  • Severe organ impairment, liver insufficiency, and renal insufficiency;
  • Complicated with tumors or hemorrhagic diseases;
  • Use of drugs forbidden to use in combination after onset, including other antiplatelet drugs, anticoagulants, thrombolytic drugs, and drugs affecting antiplatelet agents and statin metabolism.

Treatment and study plan

Intensive Drug Therapy

Other

Observational only and no predesigned interventions in this study

Other names: observational only ,no intervention

Primary outcomes

  1. Characteristics of the vessel wall

    Time frame: 3 years

    The characteristics of the vessel wall were evaluated by high-resolution magnetic resonance imaging (HR-MRI).

Secondary outcomes

  1. The change of the serum LDL-C level

    Time frame: 24 hours,14 days

    Low-density lipoprotein cholesterol (LDL-C) was tested in the laboratory before and after the treatment.

Sponsors and collaborators

Lead sponsor

Shanghai Yueyang Integrated Medicine Hospital

Other

Registry information

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Aug 18, 2023
Registry last updated
Aug 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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