NCT05897554Completed
Intra-arterial Thrombolysis After Successful Thrombectomy for Acute Ischemic Stroke in the Posterior Circulation (IAT-TOP)
Intra-arterial Thrombolysis After Successful Thrombectomy for Acute Ischemic Stroke Due to Large Vessel Occlusion in the Posterior Circulation (IAT-TOP)
Source: ClinicalTrials.gov · Last updated 13 Aug 2025
Brief summary (registry, in English)
The CHOICE study suggested that the use of adjunct intra-arterial alteplase after successful endovascular reperfusion in large vessel occlusion acute ischemic strokes may result in a greater likelihood of excellent neurological outcome at 90 days. However, CHOICE was a phase-2 trial and almost exclusively enrolled anterior circulation occlusions. Therefore, data on the safety and efficacy of post-endovascular reperfusion IAT in posterior circulation stroke is lacking. In general, anterior circulation strokes are associated with a higher risk of ICH than posterior circulation strokes. Therefore, we believe it might be safer to perform post-endovascular reperfusion IAT posterior circulation stroke. Also, there are more perforator artery in the posterior circulation, IAT would be more likely to show its benefit. Therefore, we would like to explore IA rt-PA for posterior circulation stroke after successful MT in our RCT. In this study, one interim analysis will be performed when the enrollment volume reaches 50% of the total sample size (188 cases). DSMB will determine the premature termination or continuity of research.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 247 (actual)
- First submitted
- 18 May 2023
- Start date
- 11 Aug 2023
- Primary completion date
- 27 Mar 2025
- Lead sponsor
- Xuanwu Hospital, Beijing
- Diseases
- Stroke
- NCT number
- NCT05897554
What you commit to
- Study type: Interventional
- Participants enrolled: 247
- From 11 Aug 2023 to the primary completion date, 27 Mar 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients in sedation and intubated patients could not be included if baseline NIHSS is not obtained by a neurologist or emergency physician prior to sedation or intubation;
- Systolic pressure \>185 mmHg or diastolic pressure \>110 mmHg, and cannot be controlled by antihypertensive drugs;
Other illness
- Dissection of occluded artery or intraoperative bleeding on DSA after thrombectomy;
- Seizures at stroke onset which would preclude obtaining a baseline NIHSS;
- Severe contrast allergy or absolute contraindication to iodinated contrast;
- The patient has neurological disease or mental disorder before onset, which affects the assessment of the condition;
Lab values
- Blood glucose \<50 mg/dl (2.8 mmol/L) or \>400 mg/dl (22.2 mmol/L);
- Platelet \<50\*10\^9/L, or aPTT \>40 s, or PT \>15 s;
- Known genetic or acquired bleeding diathesis, deficiency of anticoagulant factors, or oral anticoagulant drugs and INR \> 1.7, or treated with direct oral anticoagulant agents in the prior 48 hours;
- Known Severe renal Failure as defined by a serum creatinine \> 3.0 mg/dl (or 265.2 μmol/l) or glomerular Filtration Rate \[GFR\] \<30, or patient requires hemodialysis or peritoneal dialysis;
Other
- Contraindication to Intravenous Thrombolysis (except time to treatment);
- Complete clinical recovery in the angiography suite by end of MT procedure;
- More than 3 passes of thrombectomy device;
- Bilateral dilated pupils;
- Patients that cannot complete 90-day follow-up (e.g. no fixed residence, overseas patients, etc.);
- Presumed vasculitis or septic embolization;
- Suspicion of aortic dissection;
- Females who are pregnant or in lactation;
- Participating in other clinical trials that could confound the evaluation of the study;
- Other circumstances that the investigator considers inappropriate for participation or may pose a significant risk to patients.
Who the study is looking for
- Symptoms and signs compatible with ischemia in the posterior circulation;
- Basilar artery occlusion or vertebral artery occlusion without antegrade flow to the basilar artery confirmed by computed tomographic angiography (CTA)/ magnetic resonance angiography (MRA)/ digital subtraction angiography (DSA);
- Age ≥18 years and ≤80 years;
- Premorbid mRS ≤1;
- National Institutes of Health Stroke Score (NIHSS) ≥6 at admission;
- PC-ASPECTS on CT/CTA-Source Images/MRI-DWI 6-10;
- Treated with endovascular thrombectomy (EVT) resulting in an eTICI score ≥2b50 at end of the procedure;
- Time from symptom onset to randomization\<24 hours, including wake-up stroke and unwitnessed stroke; Time of onset of symptoms is defined as "last known well" (LKW) if symptoms are not witnessed or time of estimated basilar artery occlusion (defined as the time of sudden onset of basilar artery stroke symptoms, with no consideration of any preceding minor prodromal symptoms, as adjudicated by two neurologists) if symptoms are witnessed;
- Informed consent obtained from the patient or his/her legal representative.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Xuanwu Hospital, Capital Medical University Coordinator of this site? Confirm its status | Beijing | China | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.