Clinical Trials Logo

Clinical Trial Summary

This study evaluates the feasibility, safety and accuracy of a 19 gauge (19G) needle in nitinol in the performance of endoscopic ultrasound (EUS) guided transduodenal biopsy for the acquisition of samples for histologic analysis. Patients with lesions that can be approached only from the duodenum will be prospectively enrolled.


Clinical Trial Description

A 19 gauge needle in nitinol (Flex needle) has been recently become available for EUS guided procedure. The use of nitinol should guarantee a better needle flexibility with a theoretical advantage on the use of this needle for lesions that need to be sampled through the duodenum. Moreover, samples for histologic examination seems to be easy to interpret than cytologic ones allowing evaluate of the overall architecture of the tissue, better performance of immunohistochemical staining, and may be of additional value to perform tissue profiling that in the future will be very important to guide individualized therapies The existing data on the performance of the Flex needle for EUS-guided transduodenal biopsy are coming form a single study performed in one single center. Thus, the reproducibility of these results is unknown and multicenter prospective studies are warranted to answer this important question. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02307253
Study type Interventional
Source Catholic University of the Sacred Heart
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date October 2015

See also
  Status Clinical Trial Phase
Completed NCT02653469 - Augmented Pulse Pressure Variation to Predict Fluid Responsiveness in Open Laparotomy N/A
Completed NCT04032951 - 22 Gauge Needle for EUS Guided Tissue Acquisition of Samples for Histologic Examination N/A
Completed NCT01399814 - Restricted Intravenous Fluid Regime Effects on Immunological Indicators of Elderly Patients Operated for Abdominal Cancer Phase 3
Completed NCT00723216 - Japanese Efficacy and Safety Study of Enoxaparin in Patients With Curative Abdominal Cancer Surgery Phase 3
Completed NCT00186953 - Determination of a Safe Dose of Optison in Pediatric Patients With Solid Tumors Phase 1
Completed NCT03002909 - Continuous Pre-peritoneal Wound Infiltration Versus Epidural Analgesia in Cancer Surgery N/A
Recruiting NCT02557256 - Malignant Pediatric Pelvic Tumors: A Retrospective Study