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

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

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00869843
Enrollment
28
Registered
2009-03-26
Start date
2002-10-31
Completion date
2009-03-31
Last updated
2013-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Liver Tumors, Liver Metastases From Colorectal Cancer

Keywords

Metastatic colorectal cancer

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.

Interventions

PROCEDURERF Ablation

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Depth of coagulation which is possible in human liver tissue using the saline linked RF Surface ablation with the Tissue Link floating ballDay 1On day of surgery
Efficacy of the technique on surface liver tumors using saline lined RF Surface ablation.Day 1On day of surgery

Secondary

MeasureTime frameDescription
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.Day 1On day of surgery

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026