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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02965339
Other study ID # RNI2015-05 (PI2015-05)
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 2016
Est. completion date November 2018

Study information

Verified date April 2018
Source Centre Hospitalier Universitaire, Amiens
Contact Pierre-Grégoire GUINOT, Doctor
Phone 3 22 08 79 80
Email guinot.pierre-gregoire@chu-amiens.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cardiac surgery patients have many risk factors for endothelial dysfunction (hypertension, atherosclerosis, dyslipidemia, chronic renal failure ...).

It is likely that a significant number of patients suffering from a preexisting endothelial dysfunction. This endothelial dysfunction can be assessed by a molecular approach (determination of NO, ICAM1, VCAM1, IL8, endothelial microparticles ...). Extracorporeal circulation with ischemia-reperfusion causes a breach of particularly important glycocalyx as ischemia-reperfusion injury is. No studies have evaluated the time course of the infringement, and its association with the immediate post-operative complications (SIRS, coagulopathy, vasoplegic syndrome, renal failure). Only one study has regained an association between endothelial dysfunction during cardiac bypass surgery and postoperative cardiac surgery vasoplegic syndrome. A study in noncardiac surgery has regained an association between endothelial dysfunction (assessed by a vasoplegia test) and postoperative acute renal failure. Thus there is some data in the literature to suggest that the occurrence of postoperative complications (SIRS, coagulopathy, capillary leak syndrome, acute circulatory failure vasoplegic and acute renal failure) may result from the interaction between a pre-existing endothelial dysfunction and "operative" aggression (extracorporeal circulation). The onset of complications result from an interaction that depends on the importance of endothelial dysfunction at baseline.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date November 2018
Est. primary completion date September 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients = 18 years.

- Patient operated on for cardiac surgical myocardial revascularization (CABG) or surgical correction of aortic valve.

- Consent signed.

Exclusion Criteria:

- Standing arrhythmia.

- Pregnant woman.

- curative anticoagulation (warfarin, NANCO, heparin).

- Patient under guardianship.

- Patient Refused to participate.

- Cardiac surgery without CPB.

- bicuspid aortic valve.

- Participation in another study.

- preoperative sepsis.

- Minor or major, under guardianship or trusteeship (art L1121-5, L1121-8 and L1122 1-2)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU De Caen Caen

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary endpoint was the occurrence of vasoplegic syndrome The primary endpoint was the occurrence of vasoplegic syndrome correlate with markers of endothelial function following: IL8, P-selectin, von Willebrand factor precursor. 6 months
Secondary Occurrence of vasoplegic syndrome Occurrence of vasoplegic syndrome correlate with markers of endothelial function following: endothelial microparticles, Von Willebrand factor, VCAM1. 6 months
Secondary Marker of degradation glycocalyx: Marker of degradation glycocalyx: syndecan, heparan sulfate. 6 months
Secondary Inflammatory markers: Inflammatory markers: leukocytes, CRP, procalcitonin, albumin, TNF alpha, IL-10, IL-6, IL1beta 6 months
Secondary Markers of blood coagulation Markers of blood coagulation: Platelet count, PT, APTT, fibrinogen, D dimers, soluble complexes. 6 months
Secondary Complications Complications: cardiovascular (vasoplegic syndrome), kidney (KDIGO). 6 months
Secondary Death Death 6 months
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