Ignite Creation Date:
2024-05-06 @ 8:21 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06340620
Status:
RECRUITING
Last Update Posted:
2024-04-01
First Post:
2024-03-15
Brief Title:
EUS Examination Using EndoSound Vision System vs Standard Echoendoscope
Sponsor:
Orlando Health Inc
Organization:
Orlando Health Inc
Study Overview
Official Title:
Randomized Trial of Endoscopic Ultrasound Examination Using EndoSound Vision System vs Standard Echoendoscope
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a randomized trial to compare the standard echoendoscope with the newly developed EndoSound Visual System in the evaluation of lesions in the gastrointestinal tract
Detailed Description:
Endoscopic ultrasound EUS is the gold standard for evaluation and biopsy of lesions in the pancreaticobiliary tract subepithelial lesions in the gastrointestinal tract and luminal cancer staging due to its high sensitivity and specificity Endoscopic ultrasound examination is performed by echoendoscopes which are endoscopes with an ultrasound probe at the distal end to allow endoscopic ultrasound evaluation A new endoscopic ultrasound system - the EndoSound Visual System has now been developed for endoscopic ultrasound examination The EndoSound Visual System is a device that can be attached externally to upper gastrointestinal endoscopes thereby converting a standard endoscope into an echoendoscope which can then be used to perform an EUS examination
The aim of this randomized trial is to compare the standard echoendoscope with the newly developed EndoSound Visual System in the evaluation of lesions in the gastrointestinal tract
The aim of this randomized trial is to compare the standard echoendoscope with the newly developed EndoSound Visual System in the evaluation of lesions in the gastrointestinal tract
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None