Abdominal aortic aneurysm
Conditions
Interventions
Tranexamic acid 750 mg/day for 6 months after EVAR
Non-administration of Tranexamic acid
Sponsors
Morinomiya Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: EVAR cases for Abdominal aortic aneurysm Consent cases for this study
Exclusion criteria
Exclusion criteria: Rupture cases History of thrombosis Allergy for Tranexamic acid Impossible for follow up
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frequency of type II endoleak after EVAR (Number of patients) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1 Changing aneurysm size 2 Frequency of re-intervention 3 Biomarker MMP-9 IFN-r IL-6 D-dimer FDP PAI-1 TGF-B PIC | — |
Countries
Japan
Contacts
Public ContactMasaaki Kato
Morinomiya Hospital Dept. of Cardiovascular Surgery
Outcome results
None listed