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Esophagogastroduodenoscopy clinical trials

View clinical trials related to Esophagogastroduodenoscopy.

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NCT ID: NCT05504434 Completed - Gastroscopy Clinical Trials

Performance of a Single-use Gastroscope (aScope Gastro) for Esophagogastroduodenoscopy

FARE
Start date: July 4, 2022
Phase: N/A
Study type: Interventional

Several infectious outbreaks have been described in the literature as a result of contaminated endoscopes. These endoscopes cannot be sterilized and require an extensive cleaning process in which breaches of cleaning protocols, endoscope damage or the formation of biofilm can prevent proper disinfection. The risk of endoscopy associated infection (EAI) and colonization due to contaminated endoscopes is still considered to be low. However, it is likely that there is severe underreporting of outbreaks due to a lack of recognition or assuming an infection to be endogenous. Due to the sheer volume of upper-gastrointestinal endoscopy worldwide, even with a low risk of EAI, the number of affected patients is significant. In response, several manufacturers have turned to the production of single-use endoscopes that eliminate the risk of exogenous infections. There are single use duodenoscopes on the market that almost seem to match the performance of reusable duodenoscopes. A new single use sterile gastroscope, Ambu aScope gastro, has been developed whose performance has not been previously described in patients. This multicenter single arm consecutive case series study will test the performance of these single use gastroscopes in patients undergoing esophagogastroduodenoscopy.

NCT ID: NCT04720924 Completed - Clinical trials for Esophagogastroduodenoscopy

AQCS for Detection of Early Cancer and Precancerous Lesions on Upper Gastrointestinal Tract

Start date: January 16, 2021
Phase: N/A
Study type: Interventional

The purpose of our study was to assess the performance of esophagogastroduodenoscopy automatic quality-control system in real-time quality control of EGD.

NCT ID: NCT04247399 Completed - Education Clinical Trials

Simulation-assisted Teaching in Learning Gastroscopy

Start date: February 15, 2020
Phase: N/A
Study type: Interventional

This project is a single-blinded randomized controlled trial investigating the effect of simulation-based teaching in learning gastroscopy for medical doctors.

NCT ID: NCT03883035 Completed - Clinical trials for Esophagogastroduodenoscopy

Quality Control of Esophagogastroduodenoscopy Using Real-time EGD Auxiliary System

Start date: March 20, 2019
Phase: N/A
Study type: Interventional

The aim of our study was to develop an automatic quality-control system and assess the performance of this system in quality control of esophagogastroduodenoscopy.

NCT ID: NCT02215291 Completed - Clinical trials for Esophagogastroduodenoscopy

NvisionVLE™ Registry System Registry

Start date: July 2014
Phase:
Study type: Observational [Patient Registry]

Prospective, multi-site registry with longitudinal follow up for patients undergoing EGD or endoscopy. The primary objective is to provide a collection of patient NvisionVLE™ procedural data for participating physicians, including, but not limited to, imaging data, clinical utility data, demographics, pathology, treatment, and surveillance.

NCT ID: NCT01547520 Completed - Clinical trials for Esophagogastroduodenoscopy

Meperidine as the Single Sedative Agent During Esophagogastroduodenoscopy

Start date: June 2011
Phase: N/A
Study type: Interventional

Upper endoscopy is uncomfortable for most patients. Meperidine has both sedative and analgesic effects, so its use may be helpful for patients receiving upper endoscopy.

NCT ID: NCT01489891 Completed - Clinical trials for Esophagogastroduodenoscopy

Usefulness of Lidocaine as Topical Pharyngeal Anaesthesia in Esophagogastroduodenoscopy Under Sedation With Propofol

Start date: December 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the efficacy of application of the anaesthesia topical pharyngeal with lidocaine in esophagogastroduodenoscopy under propofol´s sedation, in therms of dosage and side effect´s reduction overall.