Electromagnetic Fields Versus Placebo as Third-line Therapy For Patients With Advanced Hepatocellular Carcinoma

  • STATUS
    Recruiting
  • End date
    Oct 30, 2024
  • participants needed
    166
  • sponsor
    Wake Forest University Health Sciences
Updated on 4 October 2022

Summary

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.

Description

Primary Objective: To estimate overall survival and quality of life.

Secondary Objectives

  • To estimate progression-free survival
  • To evaluate safety and tolerability in this patient population.
  • To evaluate the effect on levels of alpha-fetoprotein.

Details
Condition Hepatocellular Cancer
Treatment quality of life assessment, Placebo Device, TheraBionic Device
Clinical Study IdentifierNCT04797884
SponsorWake Forest University Health Sciences
Last Modified on4 October 2022

Eligibility

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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