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UnknownNCT01726010

22-G-Procore Needle for the Diagnosis of SETs of the Upper GI Tract

Endoscopic Ultrasound Guided Biopsy of Subepithelial Tumors of the Upper Gastrointestinal Tract Using the 22-G-Procore Needle

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Technical University of Munich · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this prospective study is to evaluate the feasibility of the 22-G Core Biopsy Needle with reverse bevel (Procore TM) in biopsy sampling of subepithelial tumors of the upper gastrointestinal tract.

Conditions

Interventions

TypeNameDescription
DEVICE22-G Procore Needle

Timeline

Start date
2012-09-01
Primary completion
2013-08-01
Completion
2013-10-01
First posted
2012-11-14
Last updated
2012-11-14

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01726010. Inclusion in this directory is not an endorsement.

22-G-Procore Needle for the Diagnosis of SETs of the Upper GI Tract (NCT01726010) · Clinical Trials Directory