New registry aims to sharpen liver tumor ablation techniques
NCT ID NCT04107766
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tracked over 1,200 people with liver cancer who received microwave ablation, a procedure that uses heat to destroy tumors. Researchers collected data over 5 years to see how well the ablation worked and how long patients lived. The goal was to create better guidelines for using this technique in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Microwave ablation (device procedure)
- What this could lead to
- If successful, this registry could provide doctors with better guidelines for using microwave ablation to treat liver tumors, potentially improving outcomes.
- What could go wrong
- This was an observational study, not a controlled trial, so it cannot prove that the ablation technique itself improves survival. The study was also terminated early, which may limit the data collected.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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1,254 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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Jun 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with at least one soft-tissue liver lesion ablated with the NEUWAVE Microwave Ablation System or NEUWAVE Microwave Ablation System with Ablation Confirmation.
- Ages
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22 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients who underwent or are scheduled to undergo a microwave ablation of one or more liver lesions with the NEUWAVE Microwave Ablation System per the device's Instructions for Use (IFU). 2. Patients with signed informed consent (or waiver approved by IRB/EC) who are willing to comply with the assessment schedule, and willing to have data included in the database. 3. Patients greater than or equal to 22 years old at the time of informed consent (or waiver approved by IRB/EC). Exclusion Criteria: 1. Patients with a life expectancy of less than 1 year, in the opinion of the treating physician. 2. Use of microwave ablation purely as a transection tool, rather than focused liver lesion ablation. 3. Patient is currently participating, or planning to participate, in another NeuWave/Ethicon-funded clinical trial or registry studying microwave ablation in the liver. Note: roll-over patients from previous NeuWave trials are permitted.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cedars Sinai Medical Center
Los Angeles, California, 90048, United States
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David Geffen School of Medicine at UCLA
Los Angeles, California, 90095, United States
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Hôpital Européen Georges-Pompidou
Paris, 75015, France
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ICAHN School of Medicine at Mount Sinai
New York, New York, 10029, United States
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Loma Linda University Medical Center
Loma Linda, California, 92354, United States
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MD Anderson Cancer Center
Houston, Texas, 77030, United States
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Mayo Clinic
Jacksonville, Florida, 32224, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Norfolk and Norwich University Hospital
Norwich, NR4 7UY, United Kingdom
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Olive View UCLA
Sylmar, California, 91342, United States
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Radboud UMC
Nijmegen, 6525 GA, Netherlands
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Renji Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, 200120, China
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Sarasota Memorial Hospital
Sarasota, Florida, 34239, United States
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Seoul National University Bundang Hospital (SNUBH)
Seongnam-si, Gyeonggi-do 13620, South Korea
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Singapore General Hospital
Singapore, 168582, Singapore
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St. James's University Hospital
Leeds, LS9 7TF, United Kingdom
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Sutter Institute for Medical Research
Sacramento, California, 95816, United States
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Tan Tock Seng Hospital
Singapore, 308433, Singapore
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Tenon Hospital
Paris, 75020, France
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The First Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, 510000, China
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The Royal Marsden Hospital
London, SW3 6JJ, United Kingdom
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Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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University Hospital Regensburg
Regensburg, 93053, Germany
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University Medical Center Goningen
Groningen, 9713 GZ, Netherlands
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University of Virginia
Charlottesville, Virginia, 22908, United States
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University of Washington Medical Center
Seattle, Washington, 98101, United States
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University of Wisconsin At Madison
Madison, Wisconsin, 53792, United States
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VUMC Amsterdam
Amsterdam, 1081 HV, Netherlands
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