Actively Recruiting
Clinical Study of Patients Treated With PuraBond Haemostatic Agent During Abdominal Aorta Open Repair
Led by IRCCS San Raffaele · Updated on 2026-03-27
100
Participants Needed
1
Research Sites
245 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Clinical Study of Patients Treated With PuraBond Haemostatic Agent During Abdominal Aorta Open Repair
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older with abdominal aortic aneurysm (pararenal, juxtarenal, infrarenal, aorto-iliac mono/bilateral)
- Use of PuraBond hemostatic agent when physician judges surgical hemostasis unsatisfactory
- Patients aged 18 years or older with steno-occlusive abdominal aortic or iliac disease
- Patients undergoing open repair surgery, including elective, urgent, and emergency cases, hospitalized and treated at San Raffaele Hospital (Milan, Italy)
- Patients able to provide informed consent for the study
You will not qualify if you...
- Patients with preoperative blood clotting or liver function abnormalities
- Patients with abdominal aortic or iliac artery disease planned for endovascular treatment
- Pregnant, breastfeeding, or planning pregnancy within 24 months
- Patients with systemic infection such as sepsis
- Patients unable or unwilling to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
IRCCS San Raffaele Hospital
Milan, Italy, Italy, 20132
Actively Recruiting
Research Team
D
Daniele Mascia, MD
CONTACT
E
Elisa Simonini, DR
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here