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Spots Global Cancer Trial Database for NOLA (NeuWave Observational Liver Ablation) Registry

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Trial Identification

Brief Title: NOLA (NeuWave Observational Liver Ablation) Registry

Official Title: A Multicenter Observational Registry to Develop Ablation Parameter Guidance for Microwave Liver Ablation of Soft Tissue Lesions

Study ID: NCT04107766

Interventions

Microwave Ablation

Study Description

Brief Summary: This is a multicenter, observational registry that follows patients for a total of 5 years from the date of the first liver ablation procedure with the NEUWAVE Microwave Ablation System.

Detailed Description: This is a multicenter, observational registry that follows patients for a total of 5 years from the date of the first liver ablation procedure with the NEUWAVE Microwave Ablation System. The data gathered from participating sites will be available to be analyzed to develop ablation parameter guidance for ablation approaches under varying patient liver tissue conditions and liver lesions. This is an "umbrella registry," which was included as an optional component in other NEUWAVE studies; hence, data from consenting patients who are or will be enrolled in other NEUWAVE soft tissue liver lesion ablation studies will be included in this registry. All other patients will be enrolled and followed prospectively, enrolled retrospectively with prospective, longitudinal follow up, or enrolled retrospectively with all retrospective follow up. Enrollment for this study will include up to 1,500 patients throughout the world who underwent or are scheduled to undergo microwave ablation of one or more soft tissue liver lesions using the NEUWAVE Microwave Ablation System or the NEUWAVE Microwave Ablation System with Ablation Confirmation.

Keywords

Eligibility

Minimum Age: 22 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Loma Linda University Medical Center, Loma Linda, California, United States

Cedars Sinai Medical Center, Los Angeles, California, United States

David Geffen School of Medicine at UCLA, Los Angeles, California, United States

Sutter Institute for Medical Research, Sacramento, California, United States

Olive View UCLA, Sylmar, California, United States

Mayo Clinic, Jacksonville, Florida, United States

University of Miami, Miller School of Medicine, Miami, Florida, United States

Sarasota Memorial Hospital, Sarasota, Florida, United States

ICAHN School of Medicine at Mount Sinai, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

MD Anderson Cancer Center, Houston, Texas, United States

University of Virginia, Charlottesville, Virginia, United States

University of Washington Medical Center, Seattle, Washington, United States

University of Wisconsin At Madison, Madison, Wisconsin, United States

The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China

Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, , China

Hôpital Européen Georges-Pompidou, Paris, , France

Tenon Hospital, Paris, , France

University Hospital Regensburg, Regensburg, , Germany

Seoul National University Bundang Hospital (SNUBH), Seongnam-si, , Korea, Republic of

Netherlands Cancer Institute (NKI), Amsterdam, , Netherlands

VUMC Amsterdam, Amsterdam, , Netherlands

University Medical Center Goningen, Groningen, , Netherlands

Radboud UMC, Nijmegen, , Netherlands

Singapore General Hospital, Singapore, , Singapore

Tan Tock Seng Hospital, Singapore, , Singapore

St. James's University Hospital, Leeds, , United Kingdom

The Royal Marsden Hospital, London, , United Kingdom

Norfolk and Norwich University Hospital, Norwich, , United Kingdom

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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