Protective Effect of Ulinastatin and Thymosin α1 Against Negative Immune Dysregulation and Organ Dysfunction After Acute Aortic Dissection Surgery (PANDA XI)
Enrolling by invitation · Not applicable
Conditions studied: Aortic Dissection, Aortic Dissection Aneurysm
In brief
Systemic inflammatory response syndrome (SIRS) and multiple organ dysfunction syndrome (MODS) are the major causes of death in patients with acute aortic syndrome (AAS). Therefore, the prevention of SIRS and MODS is of great clinical value, and immunomodulatory therapy with thymosin alpha 1 in addition to antiinflammatory treatment may be beneficial. This study was designed to test the hypothesis that the administration of Ulinastatin and Thymosin α1 during the acute phase of AAS will result in a reduced incidence of SIRS and MODS.
Key facts
- Study ID
- NCT06966687
- Run by
- Nanjing Medical University
- People needed
- 200
- Starts
- 2025-04-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-01-14
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The patients are conformed to 2010 ACC/AHA guidelines for the diagnosis and treatment of thoracic aortic disease (TAD) within two weeks of onset;
- Patients with acute aortic syndrome confirmed clinically and radiologically and planning to undergo emergency surgery were enrolled.
- The patients' age between 18 \~90 years old.
- Agree to participate in the study and sign the informed consent.
You may not qualify if…
- Patients allergic to Thymosin α1 or Ulinastatin;
- Lactating women and pregnant women;
- Patients with mental diseases, drug and alcohol dependence;
- Refuse to participate in this study and refuse to sign the informed consent.
Where it is running
- Beijing Anzhen Hospital — Beijing, Beijing Municipality, China
- The First Affiliated Hospital of Guangzhou Medical University — Guangzhou, Guangdong, China
- Shanghai East Hospital Tongji University — Shanghai, Shanghai Municipality, China
- West China Hospital — Chengdu, Sichuan, China
Full record on ClinicalTrials.gov
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