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NCT04408404 Clinical Trial

Factors Influencing Perioperative Mortality in Type A Acute Aortic Dissections Operated at Dijon University Hospital

Aortic Dissection Clinical Trial

Official title:
Factors Influencing Perioperative Mortality in Type A Acute Aortic Dissections Operated at Dijon University Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04408404
Other study ID # CCVT- Dissection
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date May 26, 2020

Study information
Verified date May 2020
Source Centre Hospitalier La Chartreuse
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Type A acute aortic dissections are a rare condition whose natural evolution is catastrophic. Global mortality remains high even if it decreased last years. This is probably due to improvement of diagnostic techniques and the evolution of surgical practices. It is however important to have medical data and statistics obtained in past years in order to better understand the factors influencing peroperative mortality and thereby to continue this improvement.

Recruitment information / eligibility
Status Completed
Enrollment 230
Est. completion date May 26, 2020
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- patients who underwent aortic dissection surgery in Dijon Burgundy University Hospital

Exclusion Criteria:

- patients who died before the surgical incision

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Acute aortic dissection
Acute aortic dissection treatment include Bentall procedure, Tyrone David procedure, Yacoub procedure or ascendant aortic replacement with or without aortic valve replacement, ascendant aortic root remodelling (all are standard of care procedures)

Locations
Country Name City State
France Cardiovascular and thoracic surgery Unit - Dijon University Hopital Dijon

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier La Chartreuse

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Monitor peri-operative mortality incidence rates Mortality during peri-operative acute aortic dissection procedure 1 day
Secondary Monitor peri-operative morbidity incidence rates Stroke, Kidney failure, Reexploration for bleeding 1 day
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