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Search / Trial NCT05927090

Outcomes of Aortic Dissection Repair

Launched by CENTRE CARDIOLOGIQUE DU NORD · Jun 23, 2023

Trial Information

Current as of November 10, 2025

Enrolling by invitation

Keywords

De Bakey Type I Dissection De Bakey Type Ii Dissection Type A Acute Aortic Dissection (Taaad) Root Sparing Replacement Ascending Aorta Replacement Partial Arch Repair Hemiarch Procedures Total Arch Replacement (Tarp) Frozen Elephant Trunk (Fet) Hemiarch Procedures Type B Acute Aortic Dissection (Tbaad) Type B Non Acute Aortic Dissection (Tbad)

ClinConnect Summary

This study (STAAD) is a large, real-world registry that follows adults undergoing surgical repair for acute type A aortic dissection (a serious tear in the chest aorta). It aims to learn how different surgical strategies (such as repairing the ascending aorta alone or with additional arch/root work, or using endovascular or open techniques) and the experience of the treating center affect short-term outcomes (like death within 30 days) and long-term outcomes (up to about 18 years). It’s observational, meaning doctors decide the best approach for each patient and researchers simply collect data on what happens.

If you or a family member might be eligible, you would be adults ages 18 to 90 who have a new acute type A dissection or related problem involving the ascending aorta, with symptoms starting within 7 days, and are undergoing their first surgical repair. Exclusions include being under 18, symptoms starting more than 7 days before surgery, prior dissection surgery, endocarditis, or trauma-related dissection. Participants will have one of several surgical options chosen by their care team, from conservative root-sparing repairs to more extensive aortic replacement, TEVAR, or open repairs. Researchers will collect information during hospital stay and follow patients over time to track outcomes such as 30-day mortality, nerve or kidney problems, bleeding, need for reoperation, and overall survival up to 18 years. The study is led by Centre Cardiologique du Nord with international collaborators and is not regulated by the FDA or testing a new drug.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients aged \> 18 years
  • TAAD or intramural hematoma involving the ascending aorta
  • Symptoms started within 7 days from surgery
  • Primary surgical repair of acute TAAD
  • Any other major cardiac surgical procedure concomitant with surgery for TAAD.
  • Exclusion Criteria:
  • Patients aged \< 18 years
  • Onset of symptoms \> 7 days from surgery
  • Prior procedure for TAAD
  • Concomitant endocarditis;
  • TAAD secondary to blunt or penetrating chest trauma.

About Centre Cardiologique Du Nord

Centre Cardiologique du Nord is a leading cardiac care institution dedicated to advancing cardiovascular health through innovative research and clinical excellence. With a focus on patient-centered care, the center actively participates in clinical trials to evaluate new therapies and interventions aimed at improving heart health outcomes. Leveraging a multidisciplinary team of experienced cardiologists, researchers, and healthcare professionals, the Centre Cardiologique du Nord is committed to contributing to the global medical community's understanding of cardiovascular diseases while ensuring the highest standards of patient safety and ethical practices in clinical research.

Locations

Saint Denis, France

Patients applied

0 patients applied

Trial Officials

Francesco Nappi, MD

Study Chair

Cardiac Surgery Centre Cardiologique du Nord de Saint-Denis, Paris, France

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported