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Tirofiban After Successful MT Recanalization in AIS

Safety and Efficacy of Adjunct Tirofiban Treatment After Successful Mechanical Thrombectomy Recanalization in Acute Anterior Circulation Ischemic Stroke- A Multicenter, Prospective, Double-blind, Randomized Trial

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06265051
Acronym
ATTRACTION
Enrollment
1380
Registered
2024-02-20
Start date
2024-04-09
Completion date
2025-12-29
Last updated
2026-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Ischemic Stroke, Vessel Occlusion

Keywords

mechanical thrombectomy, acute ischemic stroke, successful recanalization, tirofiban

Brief summary

Acute ischemic stroke with large vessel occlusion is a frequently occurring life-threatening condition. Although endovascular treatment can effectively open occluded vessels, the successful reperfusion rate exceeds 80%, but the rate of good prognosis is less than 50%. The current clinical focus is on how to improve futile recanalization. Tirofiban is widely used in the treatment of stroke, as it can effectively prevent vascular reocclusion and improve microcirculation perfusion. It has the potential to improve futile recanalization, but there is a lack of high-level evidence-based medical support. This multicenter, prospective, double-blind, randomized controlled trial was conducted to assess the effectiveness and safety of sequential tirofiban therapy following successful mechanical thrombectomy within 24 hours of onset.

Detailed description

Endovascular treatment is the primary approach for significantly improving the clinical prognosis of patients with acute large vessel occlusion, and it has been consistently recommended by both domestic and foreign guidelines. Successful vascular recanalization and restoration of ischemic tissue reperfusion are crucial for the favorable prognosis of patients with large vessel occlusion. However, the rate of successful reperfusion after endovascular treatment exceeds 80%, but the rate of favorable outcomes at 90 days follow-up is less than 50%. The reasons for ineffective recanalization include reperfusion injury, arterial reocclusion, hemorrhagic transformation, and microvascular reperfusion insufficiency. Although vascular recanalization can be visualized using DSA, not all microvascular beds can be effectively perfused, and persistent microocclusion of the capillary bed in ischemic tissue will also result in a poor prognosis. Currently, drug intervention is not commonly utilized to achieve successful recanalization after mechanical thrombectomy in clinical practice. Additionally, there is a lack of effective methods to improve ineffective recanalization. Tirofiban is widely used in the treatment of stroke, as it can effectively prevent vascular reocclusion and improve microcirculation perfusion. It has the potential to improve futile recanalization, but there is a lack of high-level evidence-based medical support. This is a prospective, randomized, multicenter, double-blind clinical trial. In 52 centers in China, 1360 patients with the following situations will be enrolled: achieved successful recanalization after mechanical thrombectomy (mTICI 2b/3) within 24h of stroke onset. Patients will be randomly assigned into 2 groups according to the ratio of 1:1: 1. experimental group received a bolus of tirofiban at a dosage of 5μg/kg (with a maximum dose not exceeding 0.5mg) through the catheter artery, followed by a continuous intravenous infusion at a rate of 0.1μg/(kg·min) for 24 hours. 2. The control group was given a placebo in the same manner. Face to face interviews will be made on baseline, 24 hours after randomization, 48 hours after randomization, day 7 after randomization or discharge day. Day 90 after randomization will be interviewed by phone or face to face. The main measure of effectiveness was the rate of mRS 0-2 after 90 days, and the primary focus on safety was the rate of symptomatic intracranial hemorrhage within 48 hours. This study aims to clarify the role of tirofiban in enhancing unsuccessful recanalization after thrombectomy, which holds significant clinical value in improving the prognosis of patients following thrombectomy.

Interventions

DRUGTirofiban

After the completion of endovascular treatment and successful recanalization (mTICI 2b/3), the patients were randomly assigned to the experimental group. Tirofiban 5μg/kg was administered intravenously through the catheter artery at a rate of 1ml/min, followed by an intravenous infusion of 0.1μg/(kg·min) for 24 hours. Standard medical treatment was administered after the surgery.

DRUGSaline placebo

After the completion of endovascular treatment and successful recanalization (mTICI 2b/3), the patients were randomly assigned to the experimental group. Saline placebo was administered in the same manner as tirofiban group. Standard medical treatment was administered after the surgery.

Sponsors

Xiang Luo
Lead SponsorOTHER
Fujian Medical University Union Hospital
CollaboratorOTHER
Jingzhou Hospital Affiliated to Yangtze University
CollaboratorUNKNOWN
Xiangyang No 1 People's Hospital Affiliated to Hubei University of Medicine
CollaboratorUNKNOWN
Puren Hospital Affiliated to Wuhan University of Science and Technology
CollaboratorOTHER
Zhongnan Hospital
CollaboratorOTHER
First Affiliated Hospital of Fujian Medical University
CollaboratorOTHER
Huazhong University of Science and Technology Tongji Medical College Affiliated Wuhan Central Hospital
CollaboratorUNKNOWN
Xianning Central Hospital
CollaboratorOTHER
Shanxi Provincial People's Hospital
CollaboratorOTHER_GOV
The Third People's Hospital of Hubei Province
CollaboratorOTHER
Jingmen Central Hospital
CollaboratorUNKNOWN
Hubei University of Medicine
CollaboratorOTHER
Wuhan No.1 Hospital
CollaboratorOTHER
Nanyang Central Hospital
CollaboratorOTHER
Yichang Central People's Hospital of China Three Gorges University
CollaboratorUNKNOWN
The Central Hospital of Huanggang
CollaboratorOTHER
Zoucheng City People's Hospital
CollaboratorUNKNOWN
Qujing Central Hospital of Yunnan Province
CollaboratorUNKNOWN
Taihe Hospital, Affiliated Hospital of Hubei Province of Medicine
CollaboratorUNKNOWN
Second Affiliated Hospital of Soochow University
CollaboratorOTHER
The First Affiliated Hospital of Nanchang University
CollaboratorOTHER
Central Hospital of Xiaogan
CollaboratorOTHER
The Central Hospital of Enshi Tujia And Miao Autonomous Prefecture
CollaboratorOTHER
Huangshi Central Hospital
CollaboratorOTHER
Zigong No.1 Peoples Hospital
CollaboratorOTHER
Xiangyang Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
The First People's Hospital of Jingzhou City
CollaboratorUNKNOWN
The First people's hospital of Xian Yang
CollaboratorUNKNOWN
Jiujiang No.1 People's Hospital
CollaboratorOTHER
Zhongxiang Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Jiangxi Provincial People's Hopital
CollaboratorOTHER
The Lichuan ethnic Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Xiangyang Central Hospital People's Hospital of Huangpi District
CollaboratorUNKNOWN
Quanzhou First Hospital
CollaboratorOTHER
Minda Hospital of Hubei Minzu University
CollaboratorUNKNOWN
The Cerebrovascular Hospital of Hubei Province
CollaboratorUNKNOWN
The First People's Hospital of Changde City
CollaboratorOTHER
Longyan First Affiliated Hospital of Fujian Medical University
CollaboratorUNKNOWN
Xiangzhou People's Hospital
CollaboratorUNKNOWN
Jingmen People's Hospital
CollaboratorUNKNOWN
The First People's Hospital of TianMen in Hubei Province
CollaboratorUNKNOWN
Hanyang Hospital, Wuhan University of Science & Technology
CollaboratorUNKNOWN
Tongcheng People's Hospital
CollaboratorUNKNOWN
Gaoyou People's Hospital
CollaboratorUNKNOWN
Zaoyang First People's Hospital
CollaboratorUNKNOWN
CR & WISCO General Hospital
CollaboratorUNKNOWN
Wuhan Hankou Hospital
CollaboratorUNKNOWN
Lu'an People's Hospital of Anhui Hospital
CollaboratorUNKNOWN
Yingtan People's Hospital
CollaboratorUNKNOWN
Shiyan Renmin Hospital
CollaboratorUNKNOWN
Dali Bai Autonomous Prefecture People's Hospital
CollaboratorUNKNOWN
Three Gorges Hospital of Chongqing University
CollaboratorOTHER
The Second People's Hospital of Jingzhou City
CollaboratorUNKNOWN
General Hospital of the Yangtze River Shipping
CollaboratorUNKNOWN
The Affiliated Hospital Of Southwest Medical University
CollaboratorOTHER
Fujian Provincial Hospital
CollaboratorOTHER
Zhongxiang People's Hospital
CollaboratorUNKNOWN
LiuZhou People's Hospital
CollaboratorOTHER
The Fifth Hospital of Wuhan
CollaboratorOTHER
Xiaogan First People's Hospital
CollaboratorUNKNOWN
Loudi Central Hospital
CollaboratorOTHER
Ezhou Central Hospital
CollaboratorUNKNOWN
Second Xiangya Hospital of Central South University
CollaboratorOTHER
Qingdao Central Hospital
CollaboratorOTHER
Taizhou First People's Hospital
CollaboratorOTHER
Renmin Hospital of Wuhan University
CollaboratorOTHER
Hubei Provincial Hospital of Integrated Chinese & Western Medicine
CollaboratorUNKNOWN
The First Affiliated Hospital of Botou Medical College
CollaboratorUNKNOWN
Xianfeng People's Hospital
CollaboratorUNKNOWN
Wuhan Third Hospital
CollaboratorOTHER
The Fourth Hospital of Wuhan
CollaboratorUNKNOWN
Chengdu Fifth People's Hospital
CollaboratorOTHER
Xingyi People's Hospital
CollaboratorUNKNOWN
Affiliated Hospital of Shandong University of Traditional Chinese Medicine
CollaboratorOTHER
Shenzhen Hospital of Southern Medical University
CollaboratorOTHER
The Third People's Hospital of Jingzhou City
CollaboratorUNKNOWN
The First People's Hospital of Jiangxia District
CollaboratorUNKNOWN
Xihua People's Hospital
CollaboratorUNKNOWN
Shanghai East Hospital
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥18 years old; 2. NIHSS score: 6-30; 3. Symptom onset to random time of 24h, including wake-up stroke or unwitnessed stroke; The onset time of symptoms was defined as the last time of normal performance. 4. mRS 0-1 before the stroke; 5. Subject or legal representative can sign an informed consent form; 6. Clinical symptoms caused by acute occlusion of the following sites confirmed by CTA or MRA: intracranial segment of ICA, M1 segment of middle cerebral artery, M2 trunk of middle cerebral artery; 7. ASPECTS≥6 on NCCT or DWI; 8. After the end of mechanical thrombectomy, the mTICI was stable at 2b/3, and there was no secondary embolism in other non-offending vessels, or the diagnostic angiography before mechanical thrombectomy showed that the occluded vessels improved to mTICI 2b/3, and no mechanical thrombectomy was planned.

Exclusion criteria

1. Intra-arterial thrombolysis; 2. Tirofiban was used within 24 hours before endovascular treatment 3. Women who are known to be pregnant or lactating, or have a positive pregnancy test before randomization; 4. Allergy to tirofiban, radiocontrast agent or Nitinol materials; 5. Any active bleeding within 30 days before stroke or recent bleeding (gastrointestinal, urinary, etc.); 6. parenchymal organ surgery or biopsy within 14 days before stroke; 7. History of heparin-induced thrombocytopenia; 8. Platelet count \< 100\*10\^9/L; 9. Being on hemodialysis or peritoneal dialysis; Known severe renal insufficiency (glomerular filtration rate \&lt; 30ml/min or serum creatinine \&gt; 220μmol/L). 10. Subjects requiring hemodialysis or peritoneal dialysis or who have contraindications to angiography for any reason; 11. The expected survival time is less than half a year (such as malignant tumors, serious heart and lung diseases, etc.); 12. Have participated in other interventional clinical studies that may have an impact on the outcome assessment; 13. Other circumstances that the investigator considers inappropriate for participation in the study or that may pose a significant risk to the patient (e.g., inability to understand and/or comply with study procedures and/or follow-up due to mental illness, cognitive or emotional disorder). 14. The midline shift of the brain or cerebral hernia, ventricular mass effect; 15. Acute intracranial hemorrhage on CT or MRI; 16. New bilateral acute stroke or intracranial multi-drainage large vessel occlusion; 17. Simple extracranial occlusion of the internal carotid artery.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients functionally independent (mRS score 0 to 2) at 90 days90 days after randomizationindependent outcome at 90 days
Number of participants with symptomatic intracranial hemorrhagewithin 48 hours of randomizationAccording to Heidelberg Bleeding Classification

Secondary

MeasureTime frameDescription
Modified ranking scale (mRS)90 days after randomizationA 0-6 scale running from perfect health without symptoms to death
Proportion of patients non-disabled (mRS score 0 to 1) or return to pre-morbid mRS score at 90 days (for patients with mRS > 1)90 days after randomizationExcellent functional outcome
Proportion of patients ambulatory or bodily needs-capable or better (mRS score 0 to 3)90 days after randomizationAmbulatory or bodily needs-capable or better
Number of participants with improvement of neurological function36 hours (24-48 hours) after randomizationProportion of patients with an NIHSS score of 0-1 or a reduction of ≥4 points from baseline at 36 hours (24-48 hours) of randomization
Health-related quality of life, assessed with the European Quality Five Dimensions Five Level scale (EQ-5D-5L)90 days after randomizationHealth-related quality of life
All-cause mortality90 days after randomizationThe ratio of total deaths from all causes to the research subjects at 90 days of randomization
Proportion of intracranial hemorrhage of any typewithin 48 hours of randomizationProportion of intracranial hemorrhage of any type within 48 hours of randomization

Countries

China

Contacts

PRINCIPAL_INVESTIGATORXiang Luo

Tongji Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026