The goal of this prospective study is to evaluate the feasibility of the 22-G Core Biopsy
Needle with reverse bevel (Procore TM) in biopsy sampling of subepithelial tumors of the
upper gastrointestinal tract.
Device: 22-G Procore Needle
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Full eligibility criteria for NCT01726010
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patient age 18 years and older
All patients with subepithelial tumors of the upper GI tract (maximum size: 3 cm)
Unable to obtain informed consent
ASA class 4 or 5
contraindication for taking biopsies
All locations for NCT01726010
Klinikum rechts der Isar
München, Bavaria, Germany, 81675
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Tris trial is registered with FDA with number: NCT01726010. The sponsor of the trial is Technische Universität München and it is looking for 20 volunteers for the current phase.
Official trial title: Endoscopic Ultrasound Guided Biopsy of Subepithelial Tumors of the Upper Gastrointestinal Tract Using the 22-G-Procore Needle
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