Thermotherapy in Addition to SOC Palliative Radiotherapy

Recruiting N/A Interventional Study
Head and Neck Squamous Cell Carcinoma Cutaneous Squamous Cell Carcinoma Breast Cancer Recurrent
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
60 (estimated)
Sponsor
King's College London · Other
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About This Trial
This study aims to investigate the efficacy and safety profile of superficial hyperthermia (wIRA) in addition to standard of care (SOC) palliative radiotherapy in patients with inoperable/incurable locally advanced or recurrent/metastatic HNSCC or cutaneous SCC superficial tumours not suitable for radical treatment. The investigators will assess the best objective response rate (ORR) of patients …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patient with histologically confirmed incurable or inoperable cancers with disease \[at least one superficial lesion(s) or lymph node(s)\] suitable for hydrosun® TWH1500 treatment 2. Patient undergoing standard of care palliative radiotherapy (suitable with the pre-specified …
Contacts

Anthony Kong

44+2078486004

Anthony.Kong@kcl.ac.uk

CONTACT

Taylor McKenzie

44+2078486004

taylor.mckenzie@kcl.ac.uk

CONTACT