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

Sponsor
Centre Hospitalier La Chartreuse (Other)
Overall Status
Completed
CT.gov ID
NCT04408404
Collaborator
(none)
230
1
28.8
8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Acute aortic dissection

Study Design

Study Type:
Observational
Actual Enrollment :
230 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Factors Influencing Perioperative Mortality in Type A Acute Aortic Dissections Operated at Dijon University Hospital
Actual Study Start Date :
Jan 1, 2018
Actual Primary Completion Date :
Jan 1, 2018
Actual Study Completion Date :
May 26, 2020

Arms and Interventions

Arm Intervention/Treatment
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

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)

Outcome Measures

Primary Outcome Measures

  1. Monitor peri-operative mortality incidence rates [1 day]

    Mortality during peri-operative acute aortic dissection procedure

Secondary Outcome Measures

  1. Monitor peri-operative morbidity incidence rates [1 day]

    Stroke, Kidney failure, Reexploration for bleeding

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients who underwent aortic dissection surgery in Dijon Burgundy University Hospital
Exclusion Criteria:
  • patients who died before the surgical incision

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cardiovascular and thoracic surgery Unit - Dijon University Hopital Dijon France 21000

Sponsors and Collaborators

  • Centre Hospitalier La Chartreuse

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
MORGANT Marie-Catherine, Principal investigator, Centre Hospitalier La Chartreuse
ClinicalTrials.gov Identifier:
NCT04408404
Other Study ID Numbers:
  • CCVT- Dissection
First Posted:
May 29, 2020
Last Update Posted:
May 29, 2020
Last Verified:
May 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 29, 2020