Evaluation of Transnasal Endoscopy During COVID-19 Pandemic

Status Recruiting

Clinical Trial Summary

Patients who received the indication for endoscopic diagnostics using gastroscopy in transnasal technique will be included into the study. The examination is carried out in standard technique and is not influenced by the study. Following the examination, patient data is collected pseudonymously and a questionnaire is submitted to the patient.

Clinical Trial Description

COVID-19 is transmitted, among other things, by a droplet infection. Conventional gastroscopy through the patient's mouth is therefore considered a high-risk examination for the medical and nursing staff. Alternatively, gastroscopy can also be performed through the patient's nose. An advantage here is that the aerosol formation is naturally significantly reduced and the patient usually does not need sedation, since in transnasal endoscopy no stranglehold occurs. Transnasal endoscopy therefore appears to us, especially during the COVID-19 pandemic, as a safe alternative to conventional gastroscopy. Patients who received the indication for endoscopic diagnostics using gastroscopy in transnasal technique will be included into the study. The examination is carried out in standard technique and is not influenced by the study. Following the examination, patient data is collected pseudonymously and a questionnaire is sumbitted to the patient. Only patients who have the indication for gastroscopy in transnasal technique are included. A specific risk to patients cannot be foreseen.This study does not interfere with diagnostics or therapy. ;

Study Design

Related Conditions & MeSH terms

Endoscopy

Clinical Trial Details

NCT number	NCT04734912
Study type	Interventional
Source	Johannes Gutenberg University Mainz
Contact	Helmut Neumann, M.D. PhD
Phone	+49 (0) 6131
Email	helmut.neumann@unimedizin-mainz.de
Status	Recruiting
Phase	N/A
Start date	January 13, 2021
Completion date	December 31, 2021

View Details

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