Coagulation Factors Alterations in Patients Undergoing Complex Thoraco-abdominal Aortic Aneurysm Repair

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Thessaly

About this trial

This study will evaluate the impact of complex thoraco-abdominal aortic aneurysm repair in coagulation during the immediate postoperative period in patients undergoing omplex thoraco-abdominal aortic aneurysm repair.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Consecutive patients undergoing complex thoraco-abdominal aortic aneurysm repair in University Hospital of Larissa, after informed consent will be included.

Disqualifiers

Refuse to participate

Prior surgery within 3 months

ASA PS > 3

Known medical history of thrombophilia or functional platelet dysfunction

Trial population

All patients will be treated by the same medical team in UHL according to the European Society for Vascular Surgery (ESVS) guidelines. Preoperatively patients will be treated with aspirin 100 mg once daily for at least 5 days. Postoperatively in the absence of bleeding patients will receive aspirin 100 mg and in the absence of neurological dysfunction due to spine ischemia they will receive clopidogrel 150 mg and from the next day dual antiplatelet therapy (aspirin 100 mg and clopidogrel 75 mg). If the patient was treated with anticoagulant agents this will be discontinued preoperative according to ACCP guidelines and it will be restarted on the 1st or 2nd postoperative day based on hemostasis. In this case patients will be treated with aspirin 100 mg once daily five days preoperatively and aspirin will also be continued postoperatively.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Patients undergoing complex thoraco-abdominal aortic aneurysm repair

    Other intervention

    Patients undergoing complex thoraco-abdominal aortic aneurysm repair

Treatment groups

58 Participants
are divided into 1 treatment group
Group A: Patients undergoing complex thoraco-abdominal aortic aneurysm repair1 intervention

Trial outcomes

Primary outcomes

1

Coagulation status

Early preoperatively, early and late postoperatively

Time frame
Day of surgery, 1st postoperative day, 4-5th postoperative day
2

Myocardial injury after non cardiac surgery

Early preoperatively, early and late postoperatively

Time frame
Day of surgery, 1st postoperative day, 4-5th postoperative day
3

Acute kidney injury

Early preoperatively, early and late postoperatively

Time frame
Day of surgery, 1st postoperative day, 4-5th postoperative day
4

Post-implantation syndrome

Early preoperatively, early and late postoperatively

Time frame
Day of surgery, 1st postoperative day, 4-5th postoperative day

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.