- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07345702
Basilar Artery Occlusion Chinese Endovascular Registry in Patients With Large-Core Infarct (BAOCHE-LC)
January 15, 2026 updated by: Chuanhui Li, Xuanwu Hospital, Beijing
Endovascular Versus Medical Therapy for Acute Large-Core Basilar Artery Occlusion: A Multicenter Retrospective Registry Study (BAOCHE-LC)
This multicenter retrospective registry study evaluates the safety and effectiveness of endovascular therapy versus medical therapy for acute large-core basilar artery occlusion.
It also investigates clinical, imaging, and laboratory factors associated with functional outcomes and mortality.
Patients are grouped according to the treatment received in routine clinical practice.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
518
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Chuanhui Li
- Phone Number: 15210439828
- Email: lichuanhui@xwh.ccmu.edu.cn
Study Locations
-
-
Beijing Municipality
-
Beijing, Beijing Municipality, China, 100053
- Xuanwu Hospital
-
Contact:
- Chuanhui Li
- Phone Number: 15210439828
- Email: lichuanhui@xwh.ccmu.edu.cn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Adults (≥18 years) with imaging-confirmed acute vertebrobasilar occlusion and large-core infarction (pc-ASPECTS 0-5) treated within 7 days of symptom onset/last known well at participating centers in China.
Patients are identified retrospectively from routine clinical practice and classified according to treatment received: endovascular therapy plus standard medical management versus standard medical management alone.
Description
Inclusion Criteria:
- Age ≥18 years, men or women.
- Occlusion (TIMI 0-1) of the basilar artery or intracranial segments of both vertebral arteries (V4) as evidenced by CTA/MRA/DSA.
- Time from symptom onset (or last known well) to treatment (endovascular therapy or medical therapy) ≤7 days.
- Patients with large core infarction in the posterior circulation, defined as a posterior circulation Acute Stroke Prognosis Early CT score (pc-ASPECTS) score of 0-5 on CT angiography source images or MR with diffusion-weighted imaging or non-contrast CT.
Exclusion Criteria:
- Subjects with occlusions in both anterior and posterior circulation.
- CT or MR evidence of hemorrhage (the presence of microbleeds on MRI is allowed).
- Missing key clinical information (e.g., unavailable baseline NIHSS, unclear symptom onset/last known well time, or missing major treatment information including whether EVT was performed).
- Baseline NIHSS score <6.
- Woman of childbearing potential who is known to be pregnant or lactating or who has a positive pregnancy test on admission.
- Missing follow-up outcomes at 90 days.
- Any other condition judged by investigators to substantially affect analysis or interpretation.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Endovascular Therapy
|
Endovascular therapy performed as part of routine clinical care for acute basilar artery occlusion, including mechanical thrombectomy with stent retriever and/or aspiration.
Rescue angioplasty and/or intracranial stenting may be used at the operator's discretion.
Peri-procedural management and concomitant medical therapy follow local standard practice.
|
|
Best Medical Treatment Alone
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of Patients Achieving mRS 0-3 at 90 Days
Time Frame: 90 days
|
The modified Rankin scale (range, 0 [no symptoms] to 6 [death]).
Higher scores mean a worse outcome.
|
90 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ordinal Shift analysis of mRS at 90 days
Time Frame: 90 days
|
The modified Rankin scale (range, 0 [no symptoms] to 6 [death])
|
90 days
|
|
Proportion of Patients Achieving mRS 0-3 at 1 year
Time Frame: 1 year
|
The modified Rankin scale (range, 0 [no symptoms] to 6 [death]).
Higher scores mean a worse outcome.
|
1 year
|
|
Rate of All-Cause Mortality at 90 Days
Time Frame: 90 days
|
Death from any cause within 90 days.
|
90 days
|
|
Rate of Symptomatic Intracranial Hemorrhage
Time Frame: 24 (-2/+12) hours
|
24 (-2/+12) hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 31, 2026
Primary Completion (Estimated)
October 31, 2026
Study Completion (Estimated)
October 31, 2026
Study Registration Dates
First Submitted
January 7, 2026
First Submitted That Met QC Criteria
January 7, 2026
First Posted (Estimated)
January 16, 2026
Study Record Updates
Last Update Posted (Actual)
January 20, 2026
Last Update Submitted That Met QC Criteria
January 15, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BAOCHE-LC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The study is proceeding.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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