← Back to all trials
Completed
NCT07043777
Three-Vessel Versus Unilateral Antegrade Cerebral Perfusion in Emergency Total Arch Replacement for Acute Type A Aortic Dissection
Conditions: Acute Type A Aortic Dissection
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 201
Sponsor: China Medical University Hospital
Location: China Medical University Hospital Taichung
Summary
This single-centre retrospective observational cohort study describes the technical feasibility of direct three-vessel antegrade cerebral perfusion, designated modified antegrade cerebral perfusion (MACP), during emergency total arch replacement for acute type A aortic dissection. MACP delivers antegrade cerebral perfusion directly to the brachiocephalic, left common carotid, and left subclavian arteries. Outcomes are summarised descriptively and compared exploratorily with unilateral right axillary antegrade cerebral perfusion (uACP). Because perfusion strategy and treating surgeon were completely confounded, the comparative analyses are intended only to contextualise the technical experience and generate hypotheses.
Eligibility Criteria
Inclusion Criteria:
* Adults aged 18 years or older.
* Patients who underwent emergency total arch replacement for acute type A aortic dissection at China Medical University Hospital between 1 January 2021 and 30 April 2025.
* Patients who received either direct three-vessel antegrade cerebral perfusion (MACP) or unilateral right axillary antegrade cerebral perfusion (uACP).
Exclusion Criteria:
* Incomplete key clinical, operative, or outcome data precluding analysis.
* Preoperative modified Rankin Scale score of 4 or higher.
* Ischemic stroke within 30 days before surgery.
* Remote prior stroke history or unavailable prior-stroke status.
* Patients managed with cerebral perfusion strategies other than MACP or uACP.
Source: ClinicalTrials.gov (NCT07043777). StuddyBuddy aggregates publicly available trial information.