The primary goal of this study is to gather efficacy data concerning overall survival with electromagnetic fields when compared to a placebo amplitude-modulated radiofrequency electromagnetic field device in subjects who have failed or are intolerant to at least two previous systemic therapies.
Primary Objective: To estimate overall survival and quality of life.
Secondary Objectives
Condition | Hepatocellular Cancer |
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Treatment | quality of life assessment, Placebo Device, TheraBionic Device |
Clinical Study Identifier | NCT04797884 |
Sponsor | Wake Forest University Health Sciences |
Last Modified on | 4 October 2022 |
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