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NCT02855879 Clinical Trial

Evaluation of the Prevalence of anomalIes of Glucose Metabolism in Patients Undergoing a Coronary Artery Bypass Graft (CABG)

Coronary Artery Bypass Graft Clinical Trial

— IMPACT  

Official title:
Evaluation of the Prevalence of anomalIes of Glucose Metabolism in Patients Undergoing a Coronary Artery Bypass Graft, Consequences for Morbi/Mortality in the Short and Medium Term

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02855879
Other study ID # VERGES 2014
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 8, 2015
Est. completion date June 5, 2019

Study information
Verified date December 2019
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to determine the prevalence of diabetes and non-diabetic glucose metabolism anomalies (glucose intolerance, non-diabetic fasting hyperglycaemia in patients about to undergo coronary artery bypass grafting (CABG).

In addition, the effect of these anomalies on post CABG morbi/mortality in the short term will be evaluated.

Recruitment information / eligibility
Status Completed
Enrollment 286
Est. completion date June 5, 2019
Est. primary completion date June 5, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- persons who have provided oral consent

- patients about to undergo coronary artery bypass grafting

- age >18 years

Exclusion Criteria:

- persons without national health insurance cover

- Adults under guardianship

- Pregnant or breast-feeding women

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Collection of biological data

• Collection of clinical data

Locations
Country Name City State
France CHU Dijon Bourgogne Dijon

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Percentage of glucose anomalies (non-diabetic fasting hyperglycaemia, glucose intolerance, diabetes) in CAD patients about to undergo coronary artery bypass grafting. Change from inclusion to week 2 and up to month 3
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