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Brief Title: MarginProbe 2.0 Data Collection Protocol
Official Title: MarginProbe 2.0 Data Collection Protocol
Study ID: NCT05377229
Brief Summary: Previous clinical studies with the MarginProbe (MP) system demonstrated the MP System diagnostic accuracy for identification of cancerous/abnormal tissue at the margins (≤ 1mm) of the ex-vivo lumpectomy specimen. The current study is a prospective data collection study with the enhanced technology, the MP2.0 System and is aimed at collecting data to optimize the system algorithm/procedure and to subsequently validate the system to demonstrate non-inferiority to the MP1.x system. In this study, MP2.0 system will be used on ex-vivo lumpectomy specimens at the Operating Room (OR). The study will collect a library of case information data using the MP2.0 system in sequential cohorts of a minimum of 50 subjects until the software and procedure are optimized. The final analysis sample size will be determined and outlined in the SAP based upon the results of the optimization stage.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Glendale Adventist Medical Center, Glendale, California, United States
Mercy Medical Center, Cedar Rapids, Iowa, United States
Logan Health Breast Center, Kalispell, Montana, United States
Englewood Health, Englewood, New Jersey, United States
Health and Hospitals Corporation/Kings County, Brooklyn, New York, United States
Northwell Northern Westchester, Mount Kisco, New York, United States
Northwell Health, Staten Island, New York, United States
Hadassah Medical Organization, Jerusalem, , Israel