Charité University Medicine Berlin
Berlin, 13353, Germany
Location status: Recruiting
Location contact
Pirus Ghadjar, Prof. Dr.
PRINCIPAL_INVESTIGATOR
Raphael Mohr, Dr.
PRINCIPAL_INVESTIGATOR
Yvonne Saewe
CONTACT
NCT Number: NCT06821958
Combined double immune checkpoint inhibition and radiofrequency electromagnetic field treatment for patients with advanced hepatocellular carcinoma
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Berlin, 13353, Germany
Location status: Recruiting
Pirus Ghadjar, Prof. Dr.
PRINCIPAL_INVESTIGATOR
Raphael Mohr, Dr.
PRINCIPAL_INVESTIGATOR
Yvonne Saewe
CONTACT
Charité University Medicine Berlin is currently the only German University Hospital with an available capacitive radiofrequency electromagnetic field treatment device. While there is retrospective data available regarding the assumed effectiveness and low toxicity profile of radiofrequency electromagnetic field treatment for various solid tumors including liver cancer, there is no prospective data available on the combined effect of first-line palliative double immune checkpoint inhibition and radiofrequency electromagnetic field treatment for patients with advanced hepatocellular carcinoma. The investigators aim to conduct a feasibility trial and plan to compare the results with data of a prospective trial with a comparable patient population who received double immune checkpoint inhibition alone.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Radiofrequency electromagnetic field treatment using a carrier frequency of 13.56 MHz
Time frame: Every 10-12 weeks until progression or a maximum follow-up of 3 years
Objective response rate
Time frame: During 4 years of trial conduction
CTCAE version 5
Time frame: During 4 years of trial conduction
European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30
Time frame: During 4 years of trial conduction
European Organisation for Research and Treatment of Cancer (EORTC) QLQ-HCC18
Time frame: During 4 years of trial conduction
Progression-free survival
Time frame: During 4 years of trial conduction
Overall survival
Time frame: During 4 years of trial conduction
Time to progression
Time frame: During 4 years of trial conduction
Duration of response
Contact information is provided by the study sponsor or research team.
Charite University, Berlin, Germany
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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