Clinical Trial

Additive Anti-inflammatory Action for Aortopathy & Arteriopathy

Recruiting
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Summary
Acute aortic syndrome (AAS) is a life-threatening condition. Inflammation plays a key role in the pathogenesis, development and progression of AAS, and is associated with significant mortality and morbidity. Understanding the inflammatory responses and inflammation resolutions is essential for an appropriate management of AAS. Twenty Chinese cardiovascular centers have collaborated to create a multicenter observational registry (named Chinese registry of Additive Anti-inflammatory Action for Aortopathy \& Arteriopathy \[5A\]), with consecutive enrollment of adult patients who underwent surgery for AAS that was started on Jan 1, 2016 and will be ended on December 31, 2040. Specially, the impact of inflammation and anti-inflammatory strategies on the early and late adverse events are investigated. Primary outcomes are severe systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), Sequential Organ Failure Assessment (SOFA) scores at 7 days following this current surgery. Secondary outcomes are SISR, 30-day mortality, operative mortality, hospital mortality, new-onset stroke, acute kidney injury, surgical site infection, reoperation for bleeding, blood transfusion and length of stay in the intensive care unit.
Protocol Amendment History 10 amendments
This ClinicalTrials.gov record has been amended 10 times since 2020-05-19; most recent amendment 2026-02-05.
Status change: Enrolling by Invitation → Recruiting 2026-02-05
Status change: Recruiting → Enrolling by Invitation 2022-08-06
Status change: Not Yet Recruiting → Recruiting 2021-01-06
Trial Details
NCT Number NCT04398992
Lead Sponsor Nanjing Medical University
Collaborators: Beijing Anzhen Hospital
Conditions Acute Aortic Syndrome
Enrollment 10,000 participants
Start Date 2016-01-01
Primary Completion 2030-12-31 (estimated)
Study Completion 2030-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-09