Aim of the present study is the evaluation of the diagnostic value of a cap assisted upper
GI-endoscopy compared to a standard upper GI-endoscopy regarding the visualisation and
evaluation of the papilla duodeni major.
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Full eligibility criteria for NCT02877797
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Indication of Esophagogastroduodenoscopy independent from the study
Age ≥ 18 years
Absence of written informed consent
Contraindication or absence of informed consent regarding sedation with Propofol
Postoperativ changes of the upper GI-tract
Intention of endoscopic intervention
Suspicion of upper GI-bleeding
Suspicion of stenosis of the esophagus
Stent in the papilla duodeni major
ASA (American Society of Anesthesiologists) classification ≥ 3
All locations for NCT02877797
Klinikum rechts der Isar der Technischen Universität München
Munich, Bavaria, Germany, 81675
View full eligibility
Tris trial is registered with FDA with number: NCT02877797. The sponsor of the trial is Technische Universität München and it is looking for 101 volunteers for the current phase.
Official trial title: The Use of Cap Assisted Forward Viewing Esophagogastroduodenoscopy to Examine the Major Duodenal Papilla
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