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Cap Assisted Forward-Viewing Endoscope vs Side-Viewing Endoscope for Examination of Major Duodenal Papilla

Not Applicable
Completed
Conditions
Duodenal Papilla, Major
Interventions
Procedure: cap assisted forward-viewing endoscope
Registration Number
NCT02883608
Lead Sponsor
Technical University of Munich
Brief Summary

Examination of major duodenal papilla (MDP) using a standard forward-viewing esophagogastroduodenoscopy (S-EGD) is limited. Until now, side-viewing duodenoscope is the modality of choice to examine the MDP. Cap assisted esophagogastroduodenoscopy (CA-EGD) uses a cap fitted to the tip of the scope that can depress the mucosal folds and thus improve visualization and examination of MDP. The aim of this study is to compare CA-EGD to side\*viewing duodenoscope for complete examination of MDP.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
63
Inclusion Criteria
  • indication for elective upper endoscopy
  • age over 18 years
  • ability to provide informed consent
Exclusion Criteria
  • surgically altered upper gastrointestinal tract
  • known or suspected upper gastrointestinal strictures
  • upper gastrointestinal bleeding
  • biliary stent
  • planned endoscopic intervention
  • American Society of Anesthesiologists class III or higher
  • contraindication for or refusal of sedation with Propofol
  • inability to give informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Initial cap assisted endoscopycap assisted forward-viewing endoscopeundergo initial cap assisted forward-viewing endoscope then side-viewing duodenoscope
Initial standard endoscopycap assisted forward-viewing endoscopeundergo initial side-viewing duodenoscope then cap assisted forward-viewing endoscope
Primary Outcome Measures
NameTimeMethod
Rate of complete visualisation of papilla duodeni majorwithin 5 minutes after intubation of the esophagus

complete visualization is defined by visualization of both proximal and distal ends together with the orifice of the papilla

Secondary Outcome Measures
NameTimeMethod
Duration needed to localize the papillawithin 5 minutes after intubation of the esophagus

Trial Locations

Locations (1)

II Medizinische Klinik am Klinikum rechts der Isar der Technischen Universität München

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Munich, Bayern, Germany

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