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

Coagulation Factors Alterations in Patients Undergoing Complex Thoraco-abdominal Aortic Aneurysm Repair (CoFA-TAAA); a Prospective Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06432387
Acronym
CoFA-TAAA
Enrollment
58
Registered
2024-05-29
Start date
2024-12-31
Completion date
2027-07-20
Last updated
2026-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coagulation Factors Alterations, Platelet Activation, Thoraco-abdominal Aortic Aneurysm Repair

Brief summary

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.

Detailed description

Endovascular aneurysm repair of abdominal aorta activates a significant inflammation reaction and has an impact on coagulation. Platelet activation seems to have a major role in this prothrombotic and hypercoagulable state. In complex thoraco-abdominal aortic aneurysm repair the implants are more complexed and the duration of operation longer. The main hypothesis is that all the above have a greater impact on platelet activation and coagulation alterations. The aim of this study is the evaluation of 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.

Interventions

OTHERPatients undergoing complex thoraco-abdominal aortic aneurysm repair

Patients undergoing complex thoraco-abdominal aortic aneurysm repair

Sponsors

University of Thessaly
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Refuse to participate * Prior surgery within 3 months * ASA PS \> 3 * Known medical history of thrombophilia or functional platelet dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Coagulation statusDay of surgery, 1st postoperative day, 4-5th postoperative dayEarly preoperatively, early and late postoperatively
Myocardial injury after non cardiac surgeryDay of surgery, 1st postoperative day, 4-5th postoperative dayEarly preoperatively, early and late postoperatively
Acute kidney injuryDay of surgery, 1st postoperative day, 4-5th postoperative dayEarly preoperatively, early and late postoperatively
Post-implantation syndromeDay of surgery, 1st postoperative day, 4-5th postoperative dayEarly preoperatively, early and late postoperatively
Major cardiovascular eventsDay of surgery, 1st postoperative day, 4-5th postoperative dayEarly preoperatively, early and late postoperatively
Major cardiovascular events, implant failure and death of any cause30 days, 3, 6, and 12 months postoperativelyEarly preoperatively, early and late postoperatively and 1 at one month

Countries

Greece

Contacts

CONTACTEleni Arnaoutoglou, Prof
earnaout@gmail.com6974301352
CONTACTMaria Ntalouka
maria.ntalouka@icloud.com
STUDY_CHAIREleni Arnaoutoglou, Prof

University of Thessaly

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 8, 2026