Efficacy of Drug-Eluting Vertebral Artery Stenting Treatment for Atherosclerotic Vertebral Arteries Stenosis
Recruiting now · Not applicable
Conditions studied: Ischemic Stroke, Vertebral Artery Stenosis
In brief
This is a prospective, multi-center, open-access, single-arm trial to observe the real-world clinical efficacy of drug-eluting vertebral artery stenting system treatment for Atherosclerotic Vertebral Arteries Stenosis. Patients will be followed at 30 days, 6, and 12 months post-procedure and annually for 1 year within 3 years.
Key facts
- Study ID
- NCT05644314
- Run by
- Nanfang Hospital, Southern Medical University
- People needed
- 144
- Starts
- 2022-05-01
- Expected to finish
- 2029-05-31
- Last updated by the study team
- 2023-03-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years old, gender is not limited;
- Patients with medically prescribed rapamycin drug-eluting vertebral artery stent systems;
- Patients and family members fully understand the trial's purpose, voluntarily participate in the trial and sign the informed consent form.
You may not qualify if…
- Unable to receive dual antiplatelet therapy due to known disease, or severe coagulation abnormalities, severe infections that are not controlled, severe systemic disease, uncontrollable hypertension, and contraindicated for surgery;
- With an aneurysm that cannot be treated earlier or simultaneously or is not suitable for surgery;
- Gastrointestinal disease with active bleeding;
- Previous myocardial infarction or large-scale cerebral infarction within 2 weeks;
- Known contraindications to heparin, rapamycin, anesthesia, and contrast agents;
- Life expectancy less than 12 months;
- the investigator judged patients to be unsuitable for participation in this study.
Where it is running
- Nanfang Hospital of Southern Medical University — Guangzhou, Guangdong, China (enrolling)
Full record on ClinicalTrials.gov
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