PuraStat® Combined With Adrenaline Versus Standard of Care in Upper Gastrointestinal Bleeding

Recruiting N/A Interventional Study
Upper Gastrointestinal Bleeding
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
126 (estimated)
Sponsor
Tallaght University Hospital · Other
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About This Trial
PuraStat® is a novel gel that offers several advantages over traditional hemostatic powders. Its transparency allows for continuous visualization of the bleeding site, and it can be applied in narrow spaces or in combination with other treatments. Additionally, the pre-filled syringe design ensures ease of handling and precise delivery. Most published data on PuraStat® as a hemostatic agent origi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age \>18 years * Undergoing endoscopic therapy for non-variceal gastrointestinal bleeding Exclusion Criteria: * Variceal or portal hypertension-related gastrointestinal bleeding * Lack of signed consent form * Pregnancy or breastfeeding
Contacts

Raquel Ballester

973705342

rballester.lleida.ics@gencat.cat

CONTACT