Status: Active
Sponsors and Collaborators: Jonsson Comprehensive Cancer Center; National Cancer Institute (NCI)
Information provided by: National Cancer Institute (NCI)
Government Identifier: NCT00024076
Condition: Lung Cancer; Malignant Mesothelioma; Metastatic Cancer; Thymoma and Thymic Carcinoma
Intervention: Procedure: radiofrequency ablation
RATIONALE: Radiofrequency ablation uses high-frequency electric current to kill tumor cells. CT-guided radiofrequency ablation may be effective treatment for lung cancer.
PURPOSE: Phase II trial to study the effectiveness of radiofrequency ablation in treating patients who have refractory or advanced lung cancer.
| Study Type: | Interventional |
| Study Design: | Treatment |
| Official Title: | Radiofrequency Ablation of Pulmonary Malignancy |
| Study Start Date: | July 2001 |
OBJECTIVES:
OUTLINE: Patients undergo percutaneous CT-guided radiofrequency ablation directly to the tumor over 2 hours.
Patients are followed at 1, 3, 6, and 12 months.
PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study.
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Diagnosis of a primary or secondary intrathoracic malignancy
PATIENT CHARACTERISTICS:
Age:
Performance status:
Life expectancy:
Hematopoietic:
Hepatic:
Renal:
PRIOR CONCURRENT THERAPY:
| United States, California | |||||
| Jonsson Comprehensive Cancer Center, UCLA | |||||
| Los Angeles, California, United States, 90095-1781 | |||||
| Jonsson Comprehensive Cancer Center |
| National Cancer Institute (NCI) |
| Study Chair: | Robert D. Suh, MD | Jonsson Comprehensive Cancer Center |
| Study ID Numbers: | CDR0000068889, UCLA-9908024, NCI-G01-2011 |
| First Received: | September 13, 2001 |
| Last Updated: | November 16, 2007 |
| ClinicalTrials.gov Identifier: | NCT00024076 |
| Health Authority: | United States: Federal Government |
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