Electroporation for Cancer Treatment Real World Registry
Condition(s) studied
Study summary
This registry aims to assess real-world long-term disease outcomes for patients treated using reversible electroporation and a chemotherapeutic or calcium; in particular tumour response rates and recurrence rates. The study also aims to characterise side effects and the occurrence of Adverse Events and their relationship to the treatment.
Eligibility
Primary outcome measure(s)
- Incidence of Treatment-Emergent Adverse Events (CTCAE) — 5 years
Safety evaluation will be performed via continuous assessment of safety parameters by reviewing events as they arise. The investigation will be put on hold if unacceptable safety issues are outstanding. Adverse Events (AE) and Serious Adverse Events (SAE) will be evaluated and graded according to Common Terminology Criteria for Adverse Events (CTCAE)
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Royal London Hospital | London | United Kingdom | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04929912 on ClinicalTrials.gov ↗ ← All trials in the UK