Abdominal Aortic Aneurysm Clinical Trial
— AAA-ITOfficial title:
Study of Thrombotic Complications After Abdominal Aortic Aneurysm Surgery With or Without Infection: AAA-IT
Verified date | April 2022 |
Source | University Hospital, Bordeaux |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
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 |
Country | Name | City | State |
---|---|---|---|
France | CHU Bordeaux | Bordeaux |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Bordeaux |
France,
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 |
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