St. Jude Children's Research Hospital
Memphis, Tennessee, 38105, United States
NCT Number: NCT00705497
Background: This prospective study was designed to be the first to evaluate the toxicity of radiofrequency ablation (RFA) in patients with recurrent pediatric solid tumors.
Methods: From 2003 through 2006, we conducted a phase I, IRB-approved study of RFA for recurrent solid tumors. A multidisciplinary cancer management team selected appropriate candidates for the study. Imaging-guided RFA was performed percutaneously. Response was assessed at 3 months. Repeat RFA was performed for some incompletely ablated or new lesions.
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Interventional
Phase 1
Memphis, Tennessee, 38105, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
General
Hepatic lesions
Musculoskeletal lesions
Lung lesions
Radiofrequency tumor ablation (RFA) is an imaging guided percutaneous or intra-operative procedure that uses a probe on the end of a sharp needle that is inserted directly into the tumor. The tumor is ablated by heating the probe (using electrical current alternating at radio frequency) which raises the temperature of the tumor potentially causing irreversible cell death.
Time frame: 5 years
St. Jude Children's Research Hospital
Other
Radiofrequency Ablation of Tumors (RFA) A Phase I Study
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