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Impact of C-arm CT in Patients With HCC Undergoing TACE: Optimal Imaging Guidance

Primary Purpose

Carcinoma, Hepatocellular

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
C-arm CT + DSA as needed
DSA only
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Carcinoma, Hepatocellular

Eligibility Criteria

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

Inclusion Criteria:

Patients must be affected by HCC

Patients must be 18 years old or older

Patients must have received an abdominal CT, PET/CT scan or MRI, completed prior to the TACE procedure.

Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

Subjects under the age of 18

Pregnant women

Sites / Locations

  • Stanford University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

C-arm CT + DSA as needed'

DSA only

Arm Description

In the group of subjects randomized in this group, the image guidance component of the procedure will be conducted by the acquisition of 3D CT-like images during a trans-hepatic arterial injection of iodinated contrast agent for road mapping the tumor feeding vessels and supplemented by DSA as needed by the operating physician as imaging guidance for planning tumor(s) treatment approach.

In the group of subjects randomized in this group, present standard of care, i.e DSA imaging only will be used by the operating physician to map out the tumor vessels and used for treatment approach. Additional 3D CT-like images will be obtained, but only used if the operator cannot perform adequate planning using DSA alone.

Outcomes

Primary Outcome Measures

Dose Area Product (DAP)
Dose area product (DAP) is a measure of the entire amount of energy (radiation dose) delivered to the patient by the beam (indicator of stochastic dose)
Cumulative Dose (CD), a Measure of Radiation Dose
CD - a measurement of total radiation to the skin (measure of a deterministic dose)

Secondary Outcome Measures

Full Information

First Posted
June 22, 2009
Last Updated
March 10, 2016
Sponsor
Stanford University
Collaborators
Siemens Healthcare Diagnostics Inc
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1. Study Identification

Unique Protocol Identification Number
NCT00926536
Brief Title
Impact of C-arm CT in Patients With HCC Undergoing TACE: Optimal Imaging Guidance
Official Title
Impact of C-arm CT in Patients With Hepatocellular Carcinoma (HCC) Undergoing Transhepatic Arterial Chemoembolization (TACE): Optimal Imaging Guidance
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
March 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
Siemens Healthcare Diagnostics Inc

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients will be enrolled based on presence of HCC and eligibility for TACE. They will be randomized to one of two arms for imaging navigation to the optimal catheter location for chemotherapy injection to treat the first (possibly sole) tumor target. The two arms will be: TACE using C-arm CT supplemented by DSA or DSA only (only DSA images will be used for navigation and tumor vessel tracking). Navigation to subsequent treatment targets in all patients will be done with fluoroscopy, CACT, and DSA, as is standard of care at Stanford University Medical Center, and is not part of the study. Vascular complexity, which affects navigation difficulty and thus the need for imaging, will be assessed separately for use in data analysis by two radiologists on a four-point scale.
Detailed Description
We hope to learn more about the utility of C-arm CT in patients undergoing TACE for HCC. Data will be evaluated with regards to: Sensitivity and specificity to diagnose additional tumors and its impact on transplantation criteria. The ability to decrease procedural time by aiding navigation through complex arterial anatomy. Impact on radiation dose. Although the patient would receive the radiation during C-arm CT, overall the number of DSA angiograms and fluroscopy may decrease, potentially negating any effect of the additional dose from C-arm CT

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Hepatocellular

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
C-arm CT + DSA as needed'
Arm Type
Experimental
Arm Description
In the group of subjects randomized in this group, the image guidance component of the procedure will be conducted by the acquisition of 3D CT-like images during a trans-hepatic arterial injection of iodinated contrast agent for road mapping the tumor feeding vessels and supplemented by DSA as needed by the operating physician as imaging guidance for planning tumor(s) treatment approach.
Arm Title
DSA only
Arm Type
Active Comparator
Arm Description
In the group of subjects randomized in this group, present standard of care, i.e DSA imaging only will be used by the operating physician to map out the tumor vessels and used for treatment approach. Additional 3D CT-like images will be obtained, but only used if the operator cannot perform adequate planning using DSA alone.
Intervention Type
Device
Intervention Name(s)
C-arm CT + DSA as needed
Other Intervention Name(s)
x-ray image intensifier, C-arm CT
Intervention Description
C-arm CT images obtained and supplemented with DSA if needed
Intervention Type
Device
Intervention Name(s)
DSA only
Other Intervention Name(s)
Standard of care
Intervention Description
DSA imaging only
Primary Outcome Measure Information:
Title
Dose Area Product (DAP)
Description
Dose area product (DAP) is a measure of the entire amount of energy (radiation dose) delivered to the patient by the beam (indicator of stochastic dose)
Time Frame
Duration of a TACE procedure, an average of 2 hours
Title
Cumulative Dose (CD), a Measure of Radiation Dose
Description
CD - a measurement of total radiation to the skin (measure of a deterministic dose)
Time Frame
Duration of a TACE procedure, an average of 2 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must be affected by HCC Patients must be 18 years old or older Patients must have received an abdominal CT, PET/CT scan or MRI, completed prior to the TACE procedure. Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: Subjects under the age of 18 Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Rebecca Fahrig
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nishita N. Kothary
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States

12. IPD Sharing Statement

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Impact of C-arm CT in Patients With HCC Undergoing TACE: Optimal Imaging Guidance

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