Clinical Study of Patients Treated With PuraBond Haemostatic Agent During Abdominal Aorta Open Repair
Recruiting now
Conditions studied: Hemostatic
In brief
Purabond Study is a physician-initiated, observational, monocentric prospective Trial. The aim of the study is to investigate the hemostatic efficacy of PuraBond for aortic anastomoses and suture lines in patients with abdominal aortic pathology (aneurysmal or steno occlusive disease) candidate to open repair at Vascular Surgery Departement - San Raffaele Hospital (Milan, Italy). The Study will include 100 patients.
Key facts
- Study ID
- NCT05733585
- Run by
- IRCCS San Raffaele
- People needed
- 100
- Starts
- 2023-02-15
- Expected to finish
- 2027-10-31
- Last updated by the study team
- 2026-03-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with ≥ 18 years of age, presenting with an abdominal aortic aneurysm (pararenal, juxtarenal, infrarenal, aorto-iliac mono/bilateral)
- Use of the Purabond hemostatic agent in patients who, in the opinion of the Physician, don't have a satisfactory surgical haemostasis
- Patients ≥ 18 years of age with steno-occlusive abdominal aortic or iliac disease
- Patients that will treated by open repair , encompassing elective, urgent and emergency presentation, hospitalized and enrolled in Vascular Surgery Unit, San Raffaele Hospital (Milan, Italy)
- Patients able to sign specific informed consent for the study
You may not qualify if…
- Patients whom exhibited preoperative derangements in haematological and coagulation profiles, and baseline derangements in liver function
- Patients with abdominal aortic and/or iliac arteries disease candidate for endovascular treatment
- Pregnant, breastfeeding, or planning on becoming pregnant within 24 months
- Systemic infection (for example: sepsis)
- Impossibility or refusal to give informed consent
Where it is running
- IRCCS San Raffaele Hospital — Milan, Italy, Italy (enrolling)
Full record on ClinicalTrials.gov
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