Simple Technique to Improve Diagnostic Yield in EUS-FNA

Sponsor
Medical College of Wisconsin (Other)
Overall Status
Completed
CT.gov ID
NCT01995474
Collaborator
(none)
60
1
2
32
1.9

Study Details

Study Description

Brief Summary

Endoscopic ultrasound and fine needle aspiration are useful tools for the diagnosis and staging of pancreatic cancer. One potential limitation is contamination when needle traverses the gastrointestinal tract under continuous negative pressure. Gastrointestinal tract contamination can lead to misinterpretation of FNA specimens. We propose a technique to eliminate any remaining negative pressure during EUS-FNA and therefore decrease gastrointestinal tract contamination. Our hypothesis is that briefly untwisting the syringe from the biopsy channel after a specimen is obtained eliminates any remaining negative pressure in the FNA needle and therefore reduces GI tract contamination of EUS-FNA specimens, and will lead to improved diagnostic accuracy of this important clinical technique.

Condition or Disease Intervention/Treatment Phase
  • Other: Twisted Syringe
  • Other: Conventional Technique
N/A

Detailed Description

Endoscopic ultrasound (EUS) has evolved into a minimally invasive diagnostic and staging method. The addition of fine needle aspiration (FNA) increases the accuracy of EUS in the diagnosis and staging of pancreatic malignancies. An ultrasound probe attached to the end of the endoscope allows real-time direct visualization by means of ultrasound transmission. During the FNA process a needle is advanced through the biopsy channel of the endoscope and into the target lesion. In order to obtain a tissue specimen of a suspicious pancreatic lesion, an FNA needle must traverse either the stomach or duodenum to access the pancreatic mass. Once the needle has entered the target lesion a syringe is exchanged for the needle stylet and negative pressure is applied allowing acquisition of a cytology specimen. Negative pressure is released from the syringe and the stop cock is closed to the syringe. However, due to the relatively long length of the needle there is is significant remaining negative pressure at the needle tip. This leads to aspiration of surrounding material including GI mucosal contamination into the needle while removing it from the target lesion.

Contamination of the FNA specimen from gastric or duodenal epithelium can occur with continued negative pressure at the needle tip upon withdrawal of the needle out of the target lesion. While EUS-FNA has a high specificity (96%), sensitivity (87%), and accuracy (94%), gastrointestinal tract contamination can lead to misinterpretation of FNA specimens. Based on clinical experience, we propose a technique to eliminate any remaining negative pressure during EUS-FNA and therefore decreasing gastrointestinal tract contamination.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Eliminating the Residual Negative Pressure in the EUS-FNA Needle Before Withdrawal Enhances the FNA Cytology Yield
Study Start Date :
Feb 1, 2010
Actual Primary Completion Date :
Oct 1, 2012
Actual Study Completion Date :
Oct 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Twisted Syringe

briefly disconnecting the syringe from the biopsy channel after a specimen is obtained and then reconnecting it

Other: Twisted Syringe
briefly disconnecting the syringe from the biopsy channel after a specimen is obtained and then reconnecting it

Active Comparator: Conventional Technique

syringe is exchanged for the needle stylet and negative pressure is applied allowing acquisition of a cytology specimen.

Other: Conventional Technique
syringe is exchanged for the needle stylet and negative pressure is applied allowing acquisition of a cytology specimen.

Outcome Measures

Primary Outcome Measures

  1. Efficacy of FNA biopsy [1 week]

    The efficacy of fine needle aspiration is assessed using on site cytopathologists who are blinded with respect to the study ARM. The efficacy of diagnostic yield from samples obtained using the needle-off technique is directly compared to the diagnostic yield of samples obtained using conventional technique.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age > 18

  • Not pregnant

  • Can give consent

  • Patients with suspicious GI lesions in need of tissue diagnosis by means of EUS/FNA

Exclusion Criteria:
  • Pregnant

  • Age < 18

  • Cannot give consent

  • EUS not technically possible

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical College of Wisconsin Milwaukee Wisconsin United States 53226

Sponsors and Collaborators

  • Medical College of Wisconsin

Investigators

  • Principal Investigator: Kulwinder Dua, MD, Medical College of Wisconsin

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical College of Wisconsin
ClinicalTrials.gov Identifier:
NCT01995474
Other Study ID Numbers:
  • PRO-00012314
First Posted:
Nov 26, 2013
Last Update Posted:
Nov 26, 2013
Last Verified:
Nov 1, 2013
Keywords provided by Medical College of Wisconsin

Study Results

No Results Posted as of Nov 26, 2013