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Study of Saline Linked Monopolar Surface Radiofrequency (RF) Ablation of Hepatic Tumors

Primary Purpose

Malignant Liver Tumors, Liver Metastases From Colorectal Cancer

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
RF Ablation
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Liver Tumors focused on measuring Metastatic colorectal cancer

Eligibility Criteria

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

Eligibility for Stage I (Normal Liver Tissue)

  • Resectable liver metastases from malignant liver tumors, primary or secondary
  • Patient has been scheduled for liver resection and is in generally good medical condition
  • No evidence of extra-hepatic disease
  • Patient does not have a pacemaker
  • Age >= 18
  • Able to provide informed consent

Eligibility for Stage II (Patients with liver metastases from colorectal cancer)

  • Resectable liver metastases from colorectal cancer
  • Patient has been scheduled for liver resection is in generally good medical condition
  • No evidence of extra-hepatic disease.
  • Patient does not have a pacemaker
  • Age >= 18
  • Able to provide informed consent

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Single group

Arm Description

Outcomes

Primary Outcome Measures

Depth of coagulation which is possible in human liver tissue using the saline linked RF Surface ablation with the Tissue Link floating ball
On day of surgery
Efficacy of the technique on surface liver tumors using saline lined RF Surface ablation.
On day of surgery

Secondary Outcome Measures

Determine a safe (non-popping upper limit) of power per area that will permit a 1 cm depth of tissue destruction without inflow occlusion and a 2 cm depth with inflow occlusion.
On day of surgery

Full Information

First Posted
March 25, 2009
Last Updated
April 22, 2013
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00869843
Brief Title
Study of Saline Linked Monopolar Surface Radiofrequency (RF) Ablation of Hepatic Tumors
Official Title
Phase I Study of Saline Linked Monopolar Surface Radiofrequency (RF) Ablation of Hepatic Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
October 2002 (undefined)
Primary Completion Date
October 2007 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To determine the depth of coagulation which is possible in human liver tissue using the saline linked RF Surface ablation with the Tissue Link floating ball. To determine the efficacy of the technique on surface liver tumors using saline linked RF surface ablati To determine a safe (non-popping upper limit) of power per area that will permit a 1 cm depth of tissue destruction without inflow occlusion an da 2 cm depth with inflow occlusion.
Detailed Description
Treatment Plan: Patients with resectable hepatic metastases confined to the liver and who are referred to the Study Chairs will undergo routine work-up for hepatic resection. Operative Procedure: Stage I will be completed and the data analyzed before Stage II commences. Stage I data will be used to define the safe levels for use in Stage II. Stage I-Depth of coagulation with and without inflow occlusion at fixed times - and powers below the popping threshold. At surgery, in the absence of extrahepatic disease, the liver will be dissected in the usual fashion for a bi-segmentectomy, hemihepatectomy or larger liver resection. Prior to transection of the liver, saline linked RF ablations will be performed on normal liver tissue within the area of resection away from the tumor and the proposed line of transection. 1 cm and 2 cm diameters will be studied together in 8 patients. They will be treated for a total of 18 minutes (9 min for 1 cm and 9 min for 2 cm with 9 minutes of inflow occlusion. The 4 cm lesions will be studied in 8 other patients, 4 of whom will receive 9 minutes of inflow occlusion. After resection of the liver and establishment of resection margins on the tumor, the ablated areas of normal liver tissue will be excised frozen and studied for depth of lesion and examined by H & E and histological techniques using vital stains that will allow definition of tissue depth. Stage II-An ablate and resect Study Once parameters have been defined on normal liver, the effect of surface RF ablation on resectable hepatic tumors which come to the surface of the liver will be examined. In this portion of the study, tumors will be treated with saline linked RF ablation with a power and a duration of application which has been found to produce the maximum safe depth of coagulation. The surface area of coagulation will be dependent upon the size of the tumor. The area of treatment will encompass the tumor as well as a zone at least 0.5cm outside the edge of the tumor. Inflow occlusion will be used in one half of the patients. After resection of the liver and establishment of resection margins on the tumor, the ablated areas will be excised frozen and studied for depth of lesion and examined by H & E and histological techniques using vital stains that will allow definition of tissue depth. Twelve tumors will be treated in 12 patients. Pathology Evaluation First Group of Patients The normal tissue exposed to RF will be resected, prepared for histo-pathological studies and examined to determine the extent of tissue necrosis and popping, if any. Second Group of Patients Tumors exposed to RF ablation will be resected and the extent of tissue necrosis and popping will be determined. Also, damage to normal tissue will be examined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Liver Tumors, Liver Metastases From Colorectal Cancer
Keywords
Metastatic colorectal cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single group
Arm Type
Other
Intervention Type
Procedure
Intervention Name(s)
RF Ablation
Primary Outcome Measure Information:
Title
Depth of coagulation which is possible in human liver tissue using the saline linked RF Surface ablation with the Tissue Link floating ball
Description
On day of surgery
Time Frame
Day 1
Title
Efficacy of the technique on surface liver tumors using saline lined RF Surface ablation.
Description
On day of surgery
Time Frame
Day 1
Secondary Outcome Measure Information:
Title
Determine a safe (non-popping upper limit) of power per area that will permit a 1 cm depth of tissue destruction without inflow occlusion and a 2 cm depth with inflow occlusion.
Description
On day of surgery
Time Frame
Day 1

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Eligibility for Stage I (Normal Liver Tissue) Resectable liver metastases from malignant liver tumors, primary or secondary Patient has been scheduled for liver resection and is in generally good medical condition No evidence of extra-hepatic disease Patient does not have a pacemaker Age >= 18 Able to provide informed consent Eligibility for Stage II (Patients with liver metastases from colorectal cancer) Resectable liver metastases from colorectal cancer Patient has been scheduled for liver resection is in generally good medical condition No evidence of extra-hepatic disease. Patient does not have a pacemaker Age >= 18 Able to provide informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven Strasberg, M.D.
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19561459
Citation
Gnerlich JL, Ritter JH, Linehan DC, Hawkins WG, Strasberg SM. Saline-linked surface radiofrequency ablation: a safe and effective method of surface ablation of hepatic metastatic colorectal cancer. Ann Surg. 2009 Jul;250(1):96-102. doi: 10.1097/SLA.0b013e3181ae91af.
Results Reference
derived
Links:
URL
http://www.siteman.wustl.edu
Description
Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine

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Study of Saline Linked Monopolar Surface Radiofrequency (RF) Ablation of Hepatic Tumors

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