Clinical Trials Directory

Trials / Completed

CompletedNCT02859883

Evaluation of Oesogastroduodenoscopy With Vision to 245 ° (Full Spectrum Endoscopy) to View the Main Disc and Accessory

Status
Completed
Phase
Study type
Observational
Enrollment
73 (actual)
Sponsor
Institut Paoli-Calmettes · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The monitoring and prognosis of patients with familial polyposis adenomatous rests on analysis of the transitional mucosa at the anal margin and especially on the tracking, characterization and resection of lesions of dysplasia type of high grade at the duodenal level, after total proctocolectomy. Currently, endoscopes with axial or lateral vision are used. The FUSE technology allows the simplification or even the improvement of patient surveillance with a 245° vision (versus150° in case of classical gastroscope). The use of a second screen to enlarge the field of view may allow both analysis of duodenum and the main and accessory papilla with one single endoscope and to decrease the number of omitted lesions .

Conditions

Interventions

TypeNameDescription
DEVICEgastroscope FUSE™All patients undergoing a diagnostic gastroscopy are eligible. Using the FUSE endoscope with side screen, the duodenal and accessory papilla are monitored. Data are collected by each operator. Clinical examination of patients is performed before they leave the centre.

Timeline

Start date
2015-03-18
Primary completion
2016-05-31
Completion
2016-05-31
First posted
2016-08-09
Last updated
2017-10-26

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02859883. Inclusion in this directory is not an endorsement.