Core Biopsy Endo Sonography Study Evaluation of the Significance of the Pro-core® Needle (COS)
Primary Purpose
Pancreatic Neoplasm
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
EUS guided FNA and fine needle punction
Sponsored by
About this trial
This is an interventional diagnostic trial for Pancreatic Neoplasm focused on measuring fine needle aspiration, core biopsy, endoscopic ultrasound, space occupying process mediastinal, perigastral, perihilar, suspect lymph nodes mediastinal, perigastral or perihilar, diagnostic accuracy of EUS guided core biopsy
Eligibility Criteria
Inclusion Criteria:
- clinical indication for endoscopic ultrasound diagnostics with fine needle biopsies
- age greater than 18 years
Exclusion Criteria:
- difficult or impossible approach to desired structures due to anatomy (postoperative anatomy, e.g.)
- cystic lesion, e.g. cystic pancreas tumors
- coagulopathy
- severe general condition of the patient
- other contraindications for endoscopical ultrasound aided fine needle punction
Sites / Locations
- Universitätsklinikum Hamburg-Eppendorf
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
EUS guided FNA and fine needle punction
Arm Description
punction of endosonographically identified space-occupying process with aspirating fine needle and pro core fine needle in a randomized order
Outcomes
Primary Outcome Measures
Diagnostic Accuracy
Diagnostic accuracy of Pro-core needle (22 G) will be compared to conventional fine needle aspiration (22 G). Therefore EUS-FNA with both needles is undertaken in a random order in each lesion. For Pro-core needle, a histological / cytological diagnosis and quality assessment will be made by pathologists.For Echotip aspiration needle, reference cytology evaluation is done by cytology experts.
The histopathological diagnosis after surgery or the clinical follow up of at least one year after EUS FNA is current standard.
Secondary Outcome Measures
EUS Pro Core FNA: Histology Samples
Histology (not cytology) samples for Pro-core Needle: Number of adequately evaluable histology samples
Complication Rates
Complication rates of EUS FNA
Full Information
NCT ID
NCT02181140
First Posted
July 8, 2013
Last Updated
June 5, 2019
Sponsor
Universitätsklinikum Hamburg-Eppendorf
1. Study Identification
Unique Protocol Identification Number
NCT02181140
Brief Title
Core Biopsy Endo Sonography Study Evaluation of the Significance of the Pro-core® Needle
Acronym
COS
Official Title
Prospective Evaluation of the Significance of the Pro-core® Needle in Differential Diagnosis of Tumorous and Inflammatory Processes
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The study is designed to evaluate the diagnostic accuracy of a new designed endoscopic ultrasonography (EUS) Core biopsy aspiration needle in comparison to a conventional EUS aspiration needle in GI-tumors.
Detailed Description
Endoscopic ultrasound is an established examination method for tumors of the gastrointestinal tract and the pancreas. Since imaging by itself is limited in differential diagnosis of tumors, EUS guided fine needle aspiration is seen as a valid complementary method. Since fine-needle aspiration (FNA) is mainly based on cytological diagnostics, this method is limited also because of lacking supplementary immune- histochemical diagnostics. Here, the obtainment of little histologically evaluable tissue samples (punched barrels) would be of benefit.
A new punch needle device called Pro-core needle (Cook)(22 / 19 gauges) offers the possibility of increasing numbers of valid extractions of histologically evaluable tissues due to a better targeted precision and maneuverability in comparison to other devices of that kind (tru-cut needles, e.g.). A little notch at the pinpoint allows the obtainment of little tissue samples, that will be kept within the device by aspiration.
This study compares the obtainment of tissue by Proc-core needle and conventional aspiration punction systems.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Neoplasm
Keywords
fine needle aspiration, core biopsy, endoscopic ultrasound, space occupying process mediastinal, perigastral, perihilar, suspect lymph nodes mediastinal, perigastral or perihilar, diagnostic accuracy of EUS guided core biopsy
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
56 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EUS guided FNA and fine needle punction
Arm Type
Other
Arm Description
punction of endosonographically identified space-occupying process with aspirating fine needle and pro core fine needle in a randomized order
Intervention Type
Device
Intervention Name(s)
EUS guided FNA and fine needle punction
Intervention Description
punction of a suspect area by a EUS guided fine needle as well as pro core fine needle to evacuate histology and smear biologics
Primary Outcome Measure Information:
Title
Diagnostic Accuracy
Description
Diagnostic accuracy of Pro-core needle (22 G) will be compared to conventional fine needle aspiration (22 G). Therefore EUS-FNA with both needles is undertaken in a random order in each lesion. For Pro-core needle, a histological / cytological diagnosis and quality assessment will be made by pathologists.For Echotip aspiration needle, reference cytology evaluation is done by cytology experts.
The histopathological diagnosis after surgery or the clinical follow up of at least one year after EUS FNA is current standard.
Time Frame
up to 1 year
Secondary Outcome Measure Information:
Title
EUS Pro Core FNA: Histology Samples
Description
Histology (not cytology) samples for Pro-core Needle: Number of adequately evaluable histology samples
Time Frame
day 0 and day 14
Title
Complication Rates
Description
Complication rates of EUS FNA
Time Frame
day 0 and day 14
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
clinical indication for endoscopic ultrasound diagnostics with fine needle biopsies
age greater than 18 years
Exclusion Criteria:
difficult or impossible approach to desired structures due to anatomy (postoperative anatomy, e.g.)
cystic lesion, e.g. cystic pancreas tumors
coagulopathy
severe general condition of the patient
other contraindications for endoscopical ultrasound aided fine needle punction
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Rösch, Prof. Dr.
Organizational Affiliation
University Hospital Eppendorf, Hamburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitätsklinikum Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
12. IPD Sharing Statement
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Core Biopsy Endo Sonography Study Evaluation of the Significance of the Pro-core® Needle
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