Skip to content

Efficacy and Safety of Indobufen Combined with Clopidogrel in the Treatment of Intracranial Artery Stenting

Efficacy and Safety of Indobufen Combined with Clopidogrel in the Treatment of Intracranial Artery Stenting

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098014
Enrollment
Unknown
Registered
2025-02-28
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Intracranial Aneurysm

Interventions

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1)Age between 18 and 80 years old. (2)Diagnosed with symptomatic intracranial atherosclerotic stenosis or intracranial aneurysm and scheduled for stenting therapy. (3)Modified Rankin Scale (mRS) score <= 2 at admission. (4)Capable of understanding and signing the informed consent form, and willing to participate in the study. (5)Able to cooperate with follow-up visits and evaluations.

Exclusion criteria

Exclusion criteria: (1)Patients with a severe bleeding tendency or active bleeding. (2)Pregnant or lactating women. (3)Patients allergic to aspirin, clopidogrel, indobufen, or contrast agents. (4)Patients with congenital aneurysmal cerebral vascular malformations (AVM) or other cerebrovascular abnormalities unrelated to the treatment of arterial stenosis. (5)Patients with severe hepatic or renal insufficiency. (6)Patients with severe cognitive impairment or psychiatric disorders that may affect treatment compliance or follow-up evaluations. (7)Patients in the acute phase of stroke (onset = 1 week). (8)Patients with severe cardiopulmonary diseases unsuitable for endovascular treatment. (9)Patients who have previously experienced adverse reactions or complications related to participation in endovascular treatment studies. (10)Patients with severe autoimmune diseases. (11)Patients with active infectious diseases, such as sepsis or tuberculosis. (12)Patients with autonomic nervous system disorders that may affect treatment efficacy or follow-up evaluations. (13)Patients who have previously participated in other clinical trials or experimental drug studies, unless the treatment regimen does not conflict with this study.

Design outcomes

Primary

MeasureTime frame
New ischemic stroke or TIA events;

Secondary

MeasureTime frame
New cerebral infarction lesions on imaging;Target vessel restenosis ;Cerebral hemorrhage and/or all-cause mortality ;Deep vein thrombosis (DVT) in the lower extremities ;

Countries

China

Contacts

Public ContactJiachun Liu

Beijing Hospital

jiachunliu2003@163.com+86 10 8513 6192

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026