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

Study Locations

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100053

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:

  1. Age ≥18 years, men or women.
  2. Occlusion (TIMI 0-1) of the basilar artery or intracranial segments of both vertebral arteries (V4) as evidenced by CTA/MRA/DSA.
  3. Time from symptom onset (or last known well) to treatment (endovascular therapy or medical therapy) ≤7 days.
  4. 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:

  1. Subjects with occlusions in both anterior and posterior circulation.
  2. CT or MR evidence of hemorrhage (the presence of microbleeds on MRI is allowed).
  3. 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).
  4. Baseline NIHSS score <6.
  5. Woman of childbearing potential who is known to be pregnant or lactating or who has a positive pregnancy test on admission.
  6. Missing follow-up outcomes at 90 days.
  7. 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.

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

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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