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Comparison of Back-loaded vs Preloaded Fiducial Needles in EUS-guided Fiducial Marker Placement in Pancreatic Cancer.

Primary Purpose

Pancreatic Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Back-loaded Needle (Device)
Preloaded Needle (Device)
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer focused on measuring Pancreatic cancer, Image guided radiation therapy, Fiducial marker placement, Endoscopic ultrasound

Eligibility Criteria

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

Inclusion Criteria:

• Patients with pathologically confirmed pancreatic cancer referred for image guided radiation therapy (IGRT)

Exclusion Criteria:

  • Age <18
  • Inability to consent
  • Known coagulopathy/thrombocytopenia (INR >1.5, platelets <75)
  • Patients on antiplatelet/anticoagulant medication that cannot safely be discontinued 5-7 days prior to the procedure
  • Gold allergy
  • Current infection
  • EUS evidence of vessel interfering with path of fiducial marker
  • Pregnancy

Sites / Locations

  • University of Colorado Hospital
  • Moffitt Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Back-loaded needle

Preloaded Needle

Arm Description

The patients will undergo Linear EUS and have fiducial marker placement via a traditional 22G back-loaded needle. CRFs will be used to record data for primary and secondary endpoints.

The patients will undergo Linear EUS and have fiducial marker placement via a traditional 22G preloaded needle. CRFs will be used to record data for primary and secondary endpoints.

Outcomes

Primary Outcome Measures

Procedure Duration Required for Placing the Fiducial Markers
Duration of procedure for placing fiducial markers including: Fiducial package was opened start time (start stop watch) + Fiducial placement end time (end stop watch) = Placing Fiducial Markers Time

Secondary Outcome Measures

Total Procedure Time
Total procedure time will be recorded during the procedure using a case report form (CRF) for Procedure Time
Number of Participants With Technical Success EUS Needle Visualization
EUS needle visualization during the procedure will be recorded on a CRF for Scale of Technical Success.
Technical Success
Defined as the proper placement of 3 fiducial markers in a pancreatic neoplasm in 2 different planes
Number of Participants With Visualization of Fiducials as Assessed by Radiation Oncology
Fiducial location on CT scan will be assessed at patient's radiation oncology appointments for IGRT.
Number of Participants With Inadvertent Deployment of Fiducials
Whether inadvertent deployment of fiducials occurs will be recorded on a CRF for Data Acquisition
Number of Participants With Ease of Passage of Delivery System
Ease of needle device passage through EUS will be recorded on a CRF form for technical success.
Number of Fiducials Placed
Number of fiducials placed will be recorded during the procedure using a case report form (CRF) for Fiducial Placement Data

Full Information

First Posted
September 22, 2014
Last Updated
December 8, 2020
Sponsor
University of Colorado, Denver
Collaborators
Cook Group Incorporated
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1. Study Identification

Unique Protocol Identification Number
NCT02332863
Brief Title
Comparison of Back-loaded vs Preloaded Fiducial Needles in EUS-guided Fiducial Marker Placement in Pancreatic Cancer.
Official Title
Comparison of Traditional Back-loaded Fiducial Needles With Preloaded Fiducial Needles in EUS-guided Fiducial Marker Placement for Image-guided Radiation Therapy in Patients With Pancreatic Cancer: A Multicenter Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
August 3, 2016 (Actual)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
May 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
Cook Group Incorporated

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Endoscopic ultrasound (EUS) has been pivotal in accomplishing image guided radiation therapy (IGRT) in patients with pancreatic cancer by allowing precise contouring and identification of target lesions in the pancreas via placement of fiducials using fine needle aspiration (FNA) needles. Currently, back-loading the fiducials is the only option for preparing delivery of fiducials via the EUS approach. A prototype 22-Gauge EUS needle preloaded with four fiducials has recently been developed, and used in a porcine models with successful results. There are no randomized controlled trials comparing total duration of time needed for placement of fiducials using technical success of the traditional back- loading technique of fiducial markers to the new preloaded needles in regards to EUS based fiducial marker placement for IGRT in pancreatic cancer. Hypotheses Use of a 22 G preloaded needle for EUS guided fiducial marker placement in patients with pancreatic cancer will: Be delivered in at least require 60% less of the procedure time that it takes for traditional back-loaded 22G needles Improve overall procedure efficiency Maintain comparable technical success and adverse event rates. Primary Aims 1) To compare the procedure time of 22G needle placement of three Visicoil (brand of flexible linear back-loaded fiducial markers) fiducial markers and 22G needle preloaded fiducial markers. Secondary Aims To compare adverse event rates in 22G needle placement of Visicoil fiducial markers and 22G needle preloaded fiducial markers To compare endpoints of technical success defined as proper placement of two to three fiducial markers in a pancreatic neoplasm in 22G needle placement of Visicoil fiducial markers and 22G needle preloaded fiducial markers.
Detailed Description
Pancreatic cancer is the twelfth most common cancer worldwide. Neoadjuvant chemoradiation therapy in patients with borderline resectable pancreatic adenocarcinoma has become standard of care and is associated with higher rates of complete resection ultimately with improvement of overall survival in this patient population. Radiation therapy to a soft tissue organ such as the pancreas can be difficult, as it is not readily visualized radiographically. Image guided radiation therapy (IGRT) is a commonly implemented modality for delivering high doses of radiation directed at cancer tissue, while reducing collateral damage to adjacent healthy tissue. Fiducials, which are inert radiographic markers typically made from gold or carbon, can be placed in and around the tumor to delineate tumor margins to allow for IGRT Endoscopic ultrasound (EUS) has been pivotal in accomplishing IGRT by allowing precise contouring and identification of target lesions in the pancreas via placement of fiducials. This has traditionally been accomplished with the use of 19-gauge or 22-gauge fine needle aspiration (FNA) needles. To prepare the needle for fiducial placement, one to two fiducials are manually back-loaded into the tip of the needle after the stylet has been removed. In order to hold the fiducials within the needle, sterile lubrication or bone wax can be applied. Once the pancreatic mass has been targeted, fiducial injection can be accomplished via stylet reinsertion or sterile water injection. Currently, back-loading the fiducials is the only option for preparing delivery of fiducials via the EUS approach. Difficulties associated with fiducial loading and deployment can increase procedure duration due to cumbersome fiducial back-loading, fiducial misplacement & migration, as well as inability to pass the fiducial marker through the needle due to endoscope angulation. Observational studies have sited a technical success rate of 86-100% using 19 and/or 22 gauge needles with average procedure time between 7-12 minutes using the fiducial back-loading technique. A new mode of fiducial delivery has recently been developed that hopes to circumvent some of the technical issues inherent to traditional fiducial marker loading and deployment. A prototype 22-Gauge EUS needle preloaded with four fiducials has been used in a porcine models with successful deployment 95.6% of the time all accurate on predetermined targets. They were deemed easy to pass, relatively easy to deploy, and easily visualized on EUS, with excellent fluoroscopic and CT visualization. In addition, time for deployment was on average less than 60 seconds. To date, there is no randomized controlled trials comparing total duration of time needed for placement of fiducials using technical success of the traditional back- loading technique of fiducial markers to the new preloaded needles in regards to EUS based fiducial marker placement for IGRT in pancreatic cancer. This will be a multicenter randomized controlled trial. Randomization be performed and patients will undergo Linear EUS and have fiducial marker placement via a traditional 22G back-loaded needle (Visicoil) or the new 22G preloaded needle (PreLoad4). Multiple endpoints will be recorded, including total length of procedure, how many markers are successfully deployed, and technical success (Ease of passage of delivery system, ease of deployment of fiducials, EUS visualization of delivery system needle, EUS visual appearance of fiducials, and time for fiducial placement defined as starting at time of removing the needle from its packaging and ending time as removal of needle after final marker deployment). Fiducial marker location will be confirmed via fluoroscopy at time of placement and on 4D treatment planning CT ordered by the radiation oncologist for simulation. Patients will be discharged home after post procedure recovery. Patients will be contacted at home by a research coordinator or endoscopy staff 24-48 hours and 7-10 days after the procedure to document any immediate and delayed complications. Patients will return for their IGRT visit, and any evidence of fiducial marker migration will be recorded by the radiation oncologist. Hypotheses Use of a 22 G preloaded needle for EUS guided fiducial marker placement in patients with pancreatic cancer will: Be delivered in at least require 60% less of the procedure time that it takes for traditional back-loaded 22G needles Improve overall procedure efficiency Maintain comparable technical success and adverse event rates. Primary Aims 1) To compare the procedure time of 22G needle placement of three Visicoil fiducial markers and 22G needle preloaded fiducial markers. Secondary Aims To compare adverse event rates in 22G needle placement of Visicoil fiducial markers and 22G needle preloaded fiducial markers To compare endpoints of technical success defined as proper placement of two to three fiducial markers in a pancreatic neoplasm in 22G needle placement of Visicoil fiducial markers and 22G needle preloaded fiducial markers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
Pancreatic cancer, Image guided radiation therapy, Fiducial marker placement, Endoscopic ultrasound

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Back-loaded needle
Arm Type
Active Comparator
Arm Description
The patients will undergo Linear EUS and have fiducial marker placement via a traditional 22G back-loaded needle. CRFs will be used to record data for primary and secondary endpoints.
Arm Title
Preloaded Needle
Arm Type
Experimental
Arm Description
The patients will undergo Linear EUS and have fiducial marker placement via a traditional 22G preloaded needle. CRFs will be used to record data for primary and secondary endpoints.
Intervention Type
Device
Intervention Name(s)
Back-loaded Needle (Device)
Intervention Description
Fiducial marker placement via a traditional 22G back-loaded needle will be performed with multiple endpoints recorded: total length of procedure how many markers are successfully deployed technical success Fiducial marker location will be confirmed via fluoroscopy at time of placement and on 4D treatment planning CT ordered by the radiation oncologist for simulation.
Intervention Type
Device
Intervention Name(s)
Preloaded Needle (Device)
Intervention Description
Fiducial marker placement via a novel 22G preloaded needle will be performed with multiple endpoints recorded: total length of procedure how many markers are successfully deployed technical success Fiducial marker location will be confirmed via fluoroscopy at time of placement and on 4D treatment planning CT ordered by the radiation oncologist for simulation.
Primary Outcome Measure Information:
Title
Procedure Duration Required for Placing the Fiducial Markers
Description
Duration of procedure for placing fiducial markers including: Fiducial package was opened start time (start stop watch) + Fiducial placement end time (end stop watch) = Placing Fiducial Markers Time
Time Frame
During scheduled procedure (approximately 1 hour)
Secondary Outcome Measure Information:
Title
Total Procedure Time
Description
Total procedure time will be recorded during the procedure using a case report form (CRF) for Procedure Time
Time Frame
During scheduled procedure (approximately 1 hour)
Title
Number of Participants With Technical Success EUS Needle Visualization
Description
EUS needle visualization during the procedure will be recorded on a CRF for Scale of Technical Success.
Time Frame
During scheduled procedure (approximately 1 hour)
Title
Technical Success
Description
Defined as the proper placement of 3 fiducial markers in a pancreatic neoplasm in 2 different planes
Time Frame
During scheduled procedure (approximately 1 hour)
Title
Number of Participants With Visualization of Fiducials as Assessed by Radiation Oncology
Description
Fiducial location on CT scan will be assessed at patient's radiation oncology appointments for IGRT.
Time Frame
Several hours to 7 days after fiducial marker deployment
Title
Number of Participants With Inadvertent Deployment of Fiducials
Description
Whether inadvertent deployment of fiducials occurs will be recorded on a CRF for Data Acquisition
Time Frame
During scheduled procedure (approximately 1 hour)
Title
Number of Participants With Ease of Passage of Delivery System
Description
Ease of needle device passage through EUS will be recorded on a CRF form for technical success.
Time Frame
During scheduled procedure (approximately 1 hour)
Title
Number of Fiducials Placed
Description
Number of fiducials placed will be recorded during the procedure using a case report form (CRF) for Fiducial Placement Data
Time Frame
During scheduled procedure (about 90 minutes)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • Patients with pathologically confirmed pancreatic cancer referred for image guided radiation therapy (IGRT) Exclusion Criteria: Age <18 Inability to consent Known coagulopathy/thrombocytopenia (INR >1.5, platelets <75) Patients on antiplatelet/anticoagulant medication that cannot safely be discontinued 5-7 days prior to the procedure Gold allergy Current infection EUS evidence of vessel interfering with path of fiducial marker Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sachin Wani, MD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Colorado Hospital
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Moffitt Cancer Center
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

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Comparison of Back-loaded vs Preloaded Fiducial Needles in EUS-guided Fiducial Marker Placement in Pancreatic Cancer.

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