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Study identifier: NCT05733585 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Study of Patients Treated With PuraBond Haemostatic Agent During Abdominal Aorta Open Repair

Condition: Hemostatic  ·  Sponsor: IRCCS San Raffaele

PhaseN/A
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Daniele Mascia, MD  ·  +390226437141  ·  mascia.daniele@hsr.it

Elisa Simonini, DR  ·  +390226437141  ·  simonini.elisa@hsr.it

Always discuss trial participation with your own doctor first.

Locations (1)

IRCCS San Raffaele HospitalMilan, Italy, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT05733585