Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04408404
Recruitment Status : Completed
First Posted : May 29, 2020
Last Update Posted : May 29, 2020
Sponsor:
Information provided by (Responsible Party):
MORGANT Marie-Catherine, Centre Hospitalier La Chartreuse

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
Aortic Dissection Procedure: Acute aortic dissection

Layout table for study information
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 : January 1, 2018
Actual Primary Completion Date : January 1, 2018
Actual Study Completion Date : May 26, 2020

Resource links provided by the National Library of Medicine


Group/Cohort 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)




Primary Outcome Measures :
  1. Monitor peri-operative mortality incidence rates [ Time Frame: 1 day ]
    Mortality during peri-operative acute aortic dissection procedure


Secondary Outcome Measures :
  1. Monitor peri-operative morbidity incidence rates [ Time Frame: 1 day ]
    Stroke, Kidney failure, Reexploration for bleeding



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 99 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients who underwent aortic dissection surgery in Dijon Burgundy University Hospital since the 01 January 2007 and the 31 december 2017.
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • patients who died before the surgical incision

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04408404


Locations
Layout table for location information
France
Cardiovascular and thoracic surgery Unit - Dijon University Hopital
Dijon, France, 21000
Sponsors and Collaborators
Centre Hospitalier La Chartreuse
Layout table for additonal information
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    Key Record Dates
Last Update Posted: May 29, 2020
Last Verified: May 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: All patients are informed before surgery that all the medical data included in the medical record could be used in cardiovascular monocentric retrospective study. No data shared.

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
Layout table for MeSH terms
Aneurysm, Dissecting
Aneurysm
Vascular Diseases
Cardiovascular Diseases