Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04325373
Other study ID # CHUBX 2020/07
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 21, 2019
Est. completion date January 27, 2021

Study information

Verified date April 2022
Source University Hospital, Bordeaux
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of our study is to evaluate the incidence of post-operative thrombotic complications after abdominal aortic aneurysm surgery in the context of atherosclerosis or infectious aneurysm and its links with preoperative inflammation and hemostasis.


Description:

Abdominal aortic aneurysm (AAA) develops in the context of atherosclerosis or infection (aortitis or mycotic aneurysm). AAA and its surgery are associated with pro-thrombotic modifications of hemostasis, which persists in the post-operative period. Pro-thrombotic reactions occur in the intraluminal thrombus. Inflammatory cells recruitment is mediated by adhesion molecules from the activated endothelium, such as "vascular cell adhesion molecule-1" (VCAM-1), "intercellular adhesion molecule-1" (ICAM-1), P-selectin and E-selectin. In the setting of infection, neutrophil death process occurs, the NETosis, with the liberation of Neutrophil Extracellular Traps (NETs), containing DNA and histones. NETs are associated with thrombosis and various studies have already quantified NETosis biomarkers in plasma from patients with thrombotic disease, such as MPO-DNA (DNA coupled myeloperoxidase). In the clinical perioperative setting, patients with aortitis scheduled for AAA surgery shwoed exhibit thrombotic events. The hypothesize was that patients with aortitis have an inflammatory and hemostatic activation different from patients who develop AAA in atherosclerotic condition, and that inflammation is a risk factor of postoperative thrombotic events.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 27, 2021
Est. primary completion date January 27, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patient >18 years-old; - patient scheduled for AAA surgery by laparotomy in the vascular surgical unit at Bordeaux University Hospital; - patient who gave his/her authorization for the use of its medical data and results of blood analyses performed on residual plasma and results of aortic material analyses Exclusion Criteria: - patient who do not understand the study (not fluently French speaking or unable to give his/her consent); - patient with a pre-existing hemostatic disorder; - patient scheduled for an endovascular surgery and benefiting from a secondary laparotomy

Study Design


Locations

Country Name City State
France CHU Bordeaux Bordeaux

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary thrombotic events Incidence of thrombotic events first 7 postoperative days after AAA surgery
Secondary white blood cells white blood cells (G/L), baseline
Secondary hemoglobin hemoglobin (g/dL), baseline
Secondary platelets platelets (G/L), baseline
Secondary prothrombin time ratio prothrombin time ratio (%), baseline
Secondary INR INR baseline
Secondary aPTT ratio aPTT ratio baseline
Secondary fibrinogen fibrinogen (g/L), baseline
Secondary CRP CRP (ng/mL), baseline
Secondary interleukin-6 interleukin-6 (pg/mL), baseline
Secondary thrombin generation test thrombin generation test (lag time (min), baseline
Secondary peak peak (nM), baseline
Secondary time to peak time to peak (min), baseline
Secondary ETP ETP (nM.min), baseline
Secondary velocity index velocity index baseline
Secondary von Willebrand factor von Willebrand factor (%), baseline
Secondary soluble P-selectin soluble P-selectin (ng/mL), baseline
Secondary MPO-AND MPO-AND (% standard) baseline
Secondary atherosclerosis % of patients with preoperative atherosclerosis (number) baseline
Secondary Aspirin treatment % of patients with preoperative treatment by Aspirin (number) baseline
Secondary clamping duration clamping duration (min), baseline
Secondary bleeding bleeding (min), baseline
Secondary vascular filling vascular filling (ml), baseline
Secondary tranexamic acid administration tranexamic acid administration (g), baseline
Secondary transfusion transfusion (pack of red blood cells, plasma volume (ml), baseline
Secondary amount of fibrinogen amount of fibrinogen (g), baseline
Secondary amount of heparin amount of heparin (UI) baseline
Secondary Type of postoperative anticoagulation Type of postoperative anticoagulation: % of patients with unfractionated heparin or low-molecular-weight heparin baseline
Secondary Administration way of postoperative anticoagulation Administration way of postoperative anticoagulation: % of administration intra-venous or subcutaneously Baseline
See also
  Status Clinical Trial Phase
Active, not recruiting NCT04227054 - Abdominal Aortic Aneurysm Sac Healing and Prevention of Endoleaks N/A
Active, not recruiting NCT03687489 - Safety and Efficacy Study of Abdominal Aortic Aneurysm Stent Graft System N/A
Active, not recruiting NCT03507413 - Metformin Therapy in Non-diabetic AAA Patients Phase 2/Phase 3
Not yet recruiting NCT05756283 - The PREHAAAB Trial: Multimodal Prehabilitation for Patients Awaiting Open Abdominal Aortic Aneurysm Repair N/A
Not yet recruiting NCT04089241 - Fusion of CT Angiography With 3D Contrast Ultrasound as a Method for Follow up for Endovascular Aneurysm Repair N/A
Active, not recruiting NCT02604303 - A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms
Completed NCT02229006 - Sodium Fluoride Imaging of Abdominal Aortic Aneurysms N/A
Terminated NCT02469376 - Evaluation of a New Imagingtechnologie for Thrombosis Phase 1
Terminated NCT01843335 - Contrast-enhanced Ultrasound in Follow-up After Endovascular Aneurysm Repair N/A
Completed NCT02224794 - LIFE Study: Least Invasive Fast-Track EVAR
Completed NCT01118520 - AARDVARK (Aortic Aneurysmal Regression of Dilation: Value of ACE-Inhibition on RisK) Phase 2
Terminated NCT01425242 - Study on Anti-inflammatory Effect of Anti-hypertensive Treatment in Patients With Small AAA's and Mild Hypertension N/A
Completed NCT00746122 - Immediate Management of the Patient With Rupture : Open Versus Endovascular Repair N/A
Completed NCT03952780 - Korean Registry of Percutaneous EVAR With INCRAFT Stent Graft for the Treatment of Abdominalaortic Aneurysm (K-INCRAFT)
Completed NCT00583414 - Endovascular Exclusion of Abdominal Aortic Aneurysms in High Risk Patients N/A
Recruiting NCT05864560 - Ankura™ AAA, Cuff and AUI Stent Graft System Post-Market Clinical Follow-Up
Completed NCT01683084 - Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdominal Aortic Aneurysms Phase 4
Active, not recruiting NCT03180996 - Global Fenestrated Anaconda Clinical sTudy
Completed NCT02493296 - The Effect of Surgery on Central Aortic Pressure & haEmodynamics Study
Completed NCT03320408 - Predicting Aneurysm Growth and Rupture With Longitudinal Biomarkers