Trial · NCT07885865
Registered outcomes33
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 20 of 33
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | All-cause mortality | 30 days | Rate of death from any cause |
| Primary | Stroke, excluding transient ischemic attack (TIA) | 30 days | Rate of stroke |
| Primary | Early Paralysis, excluding paraparesis | 30 days | Rate of paralysis |
| Primary | Technical success | 24 hours | Composite of successful delivery of the device through the vasculature, successful deployment of the device at the intended location, and patient survival |
| Primary | Patency of all graft and endograft components | At hospital discharge or at 1 month | Graft and endograft patency confirmed by computed tomography (CT) imaging assessment |
| Primary | Complete sealing of the aortic pathology | At hospital discharge or at 1 month | Absence of Type Ia and IIIa/b endoleak, complete coverage of penetrating aortic ulcer (PAU) cases, and isolation of the primary entry tear in dissection cases, confirmed by CT imaging assessment |
| Secondary | Aortic-related death | Up to 36 months after the index procedure | Rate of aortic-related death |
| Secondary | Pseudoaneurysm at the treatment sites | Up to 36 months after the index procedure | Rate of pseudoaneurysm at the treatment sites |
| Secondary | Unanticipated aortic or branch-related reoperation | Up to 36 months after the index procedure | Rate of unanticipated aortic or branch-related reoperation |
| Secondary | Late endoleak | Up to 36 months after the index procedure | Rate of Type I or III endoleak confirmed by computed tomography (CT) imaging assessment |
| Secondary | Non-cardiac/non-aortic reoperations | Up to 36 months after the index procedure | Rate of non-cardiac/non-aortic reoperations |
| Secondary | Vocal cord paralysis | Up to 36 months after the index procedure | Rate of vocal cord paralysis |
| Secondary | Myocardial infarction | Up to 36 months after the index procedure | Rate of myocardial infarction |
| Secondary | Respiratory failure | Up to 36 months after the index procedure | Rate of respiratory failure |
| Secondary | Renal failure requiring dialysis | Up to 36 months after the index procedure | Rate of renal failure requiring dialysis |
| Secondary | Thromboembolic events | Up to 36 months after the index procedure | Rate of thromboembolic events |
| Secondary | Loss of patency of a graft or endovascular stent graft, including branch grafts | Up to 36 months after the index procedure | Rate of loss of patency of a graft or endovascular stent graft, including branch grafts |
| Secondary | Secondary unplanned interventions in the treated vascular segment or related to the original pathology | Up to 36 months after the index procedure | Rate of secondary unplanned interventions in the treated vascular segment or related to the original pathology |
| Secondary | Aortic rupture | Up to 36 months after the index procedure | Rate of aortic rupture |
| Secondary | Device integrity failures | Up to 36 months after the index procedure | Rate of device integrity failures confirmed by CT imaging assessment |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
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GET https://conductscience.org/api/trials/v1/NCT07885865/registered