Drug Eluting Stenting and Short Dual Antiplatelet Therapy for Preventing Recurrent Stroke in Vertebral Stenosis Registry Study
Launched by BEIJING TIANTAN HOSPITAL · Nov 8, 2024
Trial Information
Current as of August 22, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial, called the Drug Eluting Stenting and Short Dual Antiplatelet Therapy for Preventing Recurrent Stroke in Vertebral Stenosis Registry Study, is looking at how long patients need to take certain medications after receiving a special stent (a small tube that helps keep arteries open) for a condition called vertebral artery stenosis, which is a narrowing of the arteries in the neck. The goal is to determine if patients can safely take these medications for a shorter time, which could lower their risk of bleeding and make treatment easier, without causing more strokes or other serious problems.
To participate in the study, you need to be at least 18 years old and have symptoms related to the narrowing of your vertebral arteries. The researchers will be looking for patients who meet specific health criteria, so not everyone will qualify. If you do participate, you can expect to receive the stent and follow-up care, and the study will help improve future treatment options for others in similar situations. This trial is still in the planning stages and has not yet started recruiting participants.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age ≥18 years old, gender unlimited;
- • 2. Based on clinical and imaging evidence, the investigators identified patients with symptomatic vertebral atherosclerotic stenosis who met the indications for the placement of drug-eluting vertebral artery stents;
- • 3. Patients or their guardians sign informed consent.
- Exclusion Criteria:
- • 1. Severe coagulation dysfunction, serious uncontrolled infection, serious systemic disease, uncontrolled hypertension, etc., are not suitable for surgery;
- • 2. Patients with aneurysms that cannot be treated in advance or at the same time or are not suitable for surgery;
- • 3. Myocardial infarction or large-scale cerebral infarction occurred within 2 weeks;
- • 4. Combined with atrial fibrillation, or accompanied by serious heart, liver, kidney and lung diseases;
- • 5. Interventional or surgical procedures are planned within 90 days;
- • 6. Known contraindications to heparin, rapamycin, anesthesia and contrast agents;
- • 7. Life expectancy is less than 12 months;
- • 8. The researcher considers it inappropriate to participate in this study.
About Beijing Tiantan Hospital
Beijing Tiantan Hospital, affiliated with Capital Medical University, is a leading medical institution in China renowned for its expertise in neurology, neurosurgery, and various other specialties. As a prominent clinical trial sponsor, the hospital is committed to advancing medical research and improving patient outcomes through innovative studies. With a focus on high-quality clinical trials, Beijing Tiantan Hospital adheres to rigorous ethical standards and regulatory requirements, fostering collaboration with academic institutions and industry partners to facilitate the development of cutting-edge therapies and interventions. Its state-of-the-art facilities and experienced research team enable the hospital to play a pivotal role in the global medical research landscape.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, , China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported