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Comparing Newly Developed PreCore Needle With Conventional Fine Needle in Suspected Unresectable Pancreatic Cancer

Primary Purpose

Pancreatic Cancer

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
22 gauge ProCore needle aspiration
22 gauge Fine needle aspiration
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pancreatic Cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who agree to participate in research
  • 18 years of age and older patients less than 80 years old
  • Patients who have suspected unresectable pancreatic cancer in imaging studies

Exclusion Criteria:

  • Contraindication to endoscopy
  • Patients younger than 18 years old or older than 80 years old
  • Bleeding tendency
  • Cardiopulmonary dysfunction
  • Pregnancy

Sites / Locations

  • Samsung Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

22 gauge ProCore needle aspiration

22 gauge Fine needle aspiration

Arm Description

EUS-guided pancreatic mass aspiration with 22 gauge ProCore needle

EUS-guided pancreatic mass aspiration with 22 gauge Fine needle

Outcomes

Primary Outcome Measures

The rates of diagnostic sufficiency
The rates of diagnostic sufficency will be assessed by the pathologist as the proportion of definate diagnosis from cytology and histology within 2 passes of each procendure

Secondary Outcome Measures

The presence of histologic core
The presence histologic core means the gain of tissue, not clustered cells, through each procedure. It will be also assessed by the pathologist.

Full Information

First Posted
June 4, 2013
Last Updated
April 25, 2016
Sponsor
Samsung Medical Center
Collaborators
Olympus
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1. Study Identification

Unique Protocol Identification Number
NCT01876069
Brief Title
Comparing Newly Developed PreCore Needle With Conventional Fine Needle in Suspected Unresectable Pancreatic Cancer
Official Title
Comparing Newly Developed PreCore Needle With Conventional Fine Needle in Endoscopic Ultrasonography-guided Sampling of Suspected Unresectable Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center
Collaborators
Olympus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Pancreatic cancer is associated with a poor prognosis. Therefore, rapid and accurate diagnosis of a pancreatic mass is important to direct patient management. Endoscopic ultrasonography-guided fine needle aspiration (EUS-FNA) is the current standard for sampling pancreatic mass lesions, with diagnostic accuracy of 78% to 95%. But, the EUS-FNA has some limitations include stromal cell tumors and lymphomas may be difficult to diagnose. To overcome these limitations, a new needle device with ProCore reverse-bevel technology was developed recently. Aims: The objective of this prospective study is to compare the rate of diagnostic sufficiency in the EUS sampling by using newly developed ProCore needle with conventional FNA needle in suspected unresectable pancreatic cancer. We will also compare the safety, the yield of histologic core tissue and the cost-effectiveness between these modalities.
Detailed Description
Patient: Newly diagnosed pancreatic cancer patient whose cancer lesion is suspected unresectable in diagnostic imaging such as CT or MRI Procedure: Each EUS-guided FNA and ProCore aspiration will performed twice in same patient. The priority of order will be given by randomization assignment. The number of patients required: Total sixty five patients will be required.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
65 (Actual)

8. Arms, Groups, and Interventions

Arm Title
22 gauge ProCore needle aspiration
Arm Type
Active Comparator
Arm Description
EUS-guided pancreatic mass aspiration with 22 gauge ProCore needle
Arm Title
22 gauge Fine needle aspiration
Arm Type
Active Comparator
Arm Description
EUS-guided pancreatic mass aspiration with 22 gauge Fine needle
Intervention Type
Device
Intervention Name(s)
22 gauge ProCore needle aspiration
Other Intervention Name(s)
EchoTip® ProCore™ High Definition Ultrasound Biopsy Needle
Intervention Description
Pancreatic mass evaluation through the 22 gauge ProCore needle aspiration
Intervention Type
Device
Intervention Name(s)
22 gauge Fine needle aspiration
Other Intervention Name(s)
22 gauge, EN-SHOT2 Side Port Aspiration Needle
Intervention Description
Pancreatic mass evaluation through the 22 gauge Fine needle aspiration
Primary Outcome Measure Information:
Title
The rates of diagnostic sufficiency
Description
The rates of diagnostic sufficency will be assessed by the pathologist as the proportion of definate diagnosis from cytology and histology within 2 passes of each procendure
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
The presence of histologic core
Description
The presence histologic core means the gain of tissue, not clustered cells, through each procedure. It will be also assessed by the pathologist.
Time Frame
Up to 1 year
Other Pre-specified Outcome Measures:
Title
Procedure related complications
Description
Investigate the occurrence of complications such as bleeding, perforation, pancreatitis, infection. Not only complications, but the size and location of lesion, puncture routes will be assessed.
Time Frame
Up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who agree to participate in research 18 years of age and older patients less than 80 years old Patients who have suspected unresectable pancreatic cancer in imaging studies Exclusion Criteria: Contraindication to endoscopy Patients younger than 18 years old or older than 80 years old Bleeding tendency Cardiopulmonary dysfunction Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kwang Hyuck Lee, MD.
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of

12. IPD Sharing Statement

Learn more about this trial

Comparing Newly Developed PreCore Needle With Conventional Fine Needle in Suspected Unresectable Pancreatic Cancer

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