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Study identifier: NCT06896409 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Upper Gastrointestinal Bleeding  ·  Sponsor: Tallaght University Hospital

PhaseNA
Planned participants126
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 originates from surgical settings. In endoscopy, its primary applications have been in polypectomy-related hemostasis and the promotion of wound healing. Reports indicate a hemostasis success rate of 90.4%, with a recurrence rate of 10.4%. Limited data exist regarding the efficacy of PuraStat® as a hemostatic agent in upper gastrointestinal bleeding (UGIB) lesions. This study hypothesizes that PuraStat®, when combined with Adrenaline, serves as a feasible and effective first-line treatment for gastrointestinal bleeding. To evaluate this, a prospective, randomized, parallel-group, open-label clinical trial is proposed.

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

Talk to the study team

Raquel Ballester  ·  973705342  ·  rballester.lleida.ics@gencat.cat

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Arnau de Vilanova de LleidaLleida, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06896409