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Retrospective Study of Carotid Surgery in Dijon (RESCADI)

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: NCT03631381
Recruitment Status : Unknown
Verified August 2018 by Centre Hospitalier Universitaire Dijon.
Recruitment status was:  Recruiting
First Posted : August 15, 2018
Last Update Posted : August 15, 2018
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Universitaire Dijon

Study Description
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Brief Summary:

The results in carotid surgery are an indicator of the functioning of an academic surgical team, making it possible to evaluate and improve practices, as much among surgeons in training as among senior surgeons.

The indications have evolved with the development of symptomatic stenosis surgery, and results analysis has allowed us to improve our practices.

It would be of great use to have the statistics obtained in previous years to continue improving our practices.


Condition or disease
Carotid Stenosis

Study Design
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Study Type : Observational
Estimated Enrollment : 150 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Retrospective Study of Carotid Surgery in Dijon
Actual Study Start Date : September 4, 2017
Estimated Primary Completion Date : September 2019
Estimated Study Completion Date : December 2019
Groups and Cohorts
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Outcome Measures
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Primary Outcome Measures :
  1. mortality rate (%) [ Time Frame: Day 30 ]
  2. incidence of complications (%) [ Time Frame: Day 30 ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients operated for carotid stenosis in the cardiovascular and thoracic surgery department at Dijon University Hospital since 2000
Criteria

Inclusion Criteria:

all patients operated for carotid stenosis at Dijon University Hospital

Exclusion Criteria:

none

Contacts and Locations
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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): NCT03631381


Locations
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France
Chu Dijon Bourgogne Recruiting
Dijon, France, 21000
Contact: Eric STEINMETZ, MD    03.80.29.33.52    eric.steinmetz@chu-dijon.fr   
Sponsors and Collaborators
Centre Hospitalier Universitaire Dijon
More Information
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Responsible Party: Centre Hospitalier Universitaire Dijon
ClinicalTrials.gov Identifier: NCT03631381    
Other Study ID Numbers: STEINMETZ 2017
First Posted: August 15, 2018    Key Record Dates
Last Update Posted: August 15, 2018
Last Verified: August 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Carotid Stenosis
Carotid Artery Diseases
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
 Nervous System Diseases
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases