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

NCT ID: NCT04408404

Last Updated: 2020-05-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

230 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-01

Study Completion Date

2020-05-26

Brief Summary

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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.

Detailed Description

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Conditions

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Aortic Dissection

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Type A aortic dissection

Patient operated for type A acute aortic dissection between 01 January 2007 and 31 December 2017 in Dijon Burgundy University Hospital

Acute aortic dissection

Intervention Type PROCEDURE

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)

Interventions

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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)

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* patients who died before the surgical incision
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier La Chartreuse

OTHER

Sponsor Role lead

Responsible Party

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MORGANT Marie-Catherine

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Cardiovascular and thoracic surgery Unit - Dijon University Hopital

Dijon, , France

Site Status

Countries

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France

Other Identifiers

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CCVT- Dissection

Identifier Type: -

Identifier Source: org_study_id