A Study of Electromagnetic Waves in the Treatment of the Advanced Hepatocarcinoma (THBC002)
Primary Purpose
Carcinoma, Hepatocellular
Status
Terminated
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Amplitude-modulated electromagnetic fields
Sponsored by

About this trial
This is an interventional treatment trial for Carcinoma, Hepatocellular focused on measuring carcinoma, hepatocellular, electromagnetic fields
Eligibility Criteria
Inclusion Criteria:
- The patients must have a diagnosis of inoperable hepatocellular carcinoma.
- The patients who have an AFP level higher than 400 ng/ml and an appearance characteristic of cancer of the liver do not need histological confirmation. These patients must however have a negative serology for the antigen of surface of hepatitis B If serology for this antigen is positive, they must have a rate of AFP higher than 4000 ng/ml.
- Presence of one or more lesions measurable(s) according to criteria's RECIST.
Exclusion Criteria:
- Other anti-cancer treatments are not authorized during this study.
Sites / Locations
- Cabinet Médical de l'Avenue de la gare 6
Outcomes
Primary Outcome Measures
• To determine disease free survival at 4 months while receiving the experimental treatment.
Response rate
Secondary Outcome Measures
To determine the influence of the treatment on the hepatic function of patients with a diagnosis of cirrhosis. To determine the impact of the treatment by means of electromagnetic waves on the overall survival of patients.
Full Information
NCT ID
NCT00440934
First Posted
February 24, 2007
Last Updated
May 2, 2008
Sponsor
Pasche, Boris, M.D.
Collaborators
Barbault, Alexandre, M.S.
1. Study Identification
Unique Protocol Identification Number
NCT00440934
Brief Title
A Study of Electromagnetic Waves in the Treatment of the Advanced Hepatocarcinoma
Acronym
THBC002
Official Title
Étude de Phase II Pour déterminer l'efficacité Des Ondes électromagnétiques de Basse intensité administrées Par Voie Buccale Dans le Traitement du Cancer du Foie avancé
Study Type
Interventional
2. Study Status
Record Verification Date
May 2008
Overall Recruitment Status
Terminated
Why Stopped
Poor patient accrual
Study Start Date
February 2007 (undefined)
Primary Completion Date
December 2007 (Anticipated)
Study Completion Date
December 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Pasche, Boris, M.D.
Collaborators
Barbault, Alexandre, M.S.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Hepatocarcinoma (HCC) is the first cause of deaths due to cancer worldwide. More than one million two hundred thousand new patients are diagnosed each year. The prognosis of patients suffering from advanced hepatocarcinoma is poor with an average survival of less than six months. Phase I data suggest that low levels of electromagnetic fields administered intrabucally with a portable and programmable device are a safe and potentially effective treatment for advanced cancer. The device is connected to a spoon-like coupler placed in the patient's mouth during treatment. Patients with advanced HCC and limited therapeutic options will be offered treatment with a combination of frequencies.
Detailed Description
Hepatocarcinoma (HCC) is the first cause of deaths due to cancer worldwide. More than one million two hundred thousand new patients are diagnosed each year. The prognosis of patients suffering from advanced hepatocarcinoma is poor with an average survival of less than six months. Therapies for hepatocarcinoma are limited. Resection of the primary tumor is the therapeutic approach of first choice when possible. Although this intervention results in long-term survival for some patients, only a minority of them are surgical candidates because of limitations due to tumor size, patient's overall condition or presence of hepatic cirrhosis.
Phase I data suggest that low levels of amplitude-modulated electromagnetic fields administered intrabucally with a portable and programmable device are a safe and potentially effective treatment for advanced cancer. The device is connected to a spoon-like coupler placed in the patient's mouth during treatment. Patients with advanced HCC and limited therapeutic options will be offered treatment with a combination of HCC-specific frequencies.
The patients will be offered ambulatory treatment, which will be administered three times a day for 60 min until disease progression or death.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Hepatocellular
Keywords
carcinoma, hepatocellular, electromagnetic fields
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Amplitude-modulated electromagnetic fields
Primary Outcome Measure Information:
Title
• To determine disease free survival at 4 months while receiving the experimental treatment.
Time Frame
4 months
Title
Response rate
Time Frame
six months
Secondary Outcome Measure Information:
Title
To determine the influence of the treatment on the hepatic function of patients with a diagnosis of cirrhosis. To determine the impact of the treatment by means of electromagnetic waves on the overall survival of patients.
Time Frame
six months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
The patients must have a diagnosis of inoperable hepatocellular carcinoma.
The patients who have an AFP level higher than 400 ng/ml and an appearance characteristic of cancer of the liver do not need histological confirmation. These patients must however have a negative serology for the antigen of surface of hepatitis B If serology for this antigen is positive, they must have a rate of AFP higher than 4000 ng/ml.
Presence of one or more lesions measurable(s) according to criteria's RECIST.
Exclusion Criteria:
Other anti-cancer treatments are not authorized during this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Boris Pasche, MD, PhD
Organizational Affiliation
Cabinet Médical Avenue de la gare 6
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cabinet Médical de l'Avenue de la gare 6
City
Lausanne
State/Province
Vaud
ZIP/Postal Code
1003
Country
Switzerland
12. IPD Sharing Statement
Learn more about this trial
A Study of Electromagnetic Waves in the Treatment of the Advanced Hepatocarcinoma
We'll reach out to this number within 24 hrs