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Spots Global Cancer Trial Database for Pilot Study of an Implantable Microdevice for Evaluating Drug Responses in Situ in Prostate Cancer

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Trial Identification

Brief Title: Pilot Study of an Implantable Microdevice for Evaluating Drug Responses in Situ in Prostate Cancer

Official Title: Pilot Study of an Implantable Microdevice for Evaluating Drug Responses in Situ in Prostate Cancer

Study ID: NCT04399876

Interventions

Microdevice

Study Description

Brief Summary: In this research study, is assessing the feasibility of using an MR-guided implantable microdevice to measure tumor response to chemotherapy and other clinically relevant drugs in participants that have prostate cancer and are scheduled for a radical prostatectomy. The name of the study intervention involved in this study is: - Implantation of a MR-guided microdevice

Detailed Description: This research study is assessing the feasibility and safety of implanting and retrieving a 'microdevice' that releases up to 20 drugs directly within the prostate cancer lesion as a possible tool to evaluate the effectiveness of several approved cancer drugs against prostate cancer. Participants will be identified with confirmed prostate cancer whose treatment plan includes surgery as a component of standard-of-care treatment. The name of the study intervention involved in this study is: * Implantation of a MR-guided microdevice . * It is expected that about 35 people will take part in this research study; 5 in the Ex Vivo Cohort and 30 in Surgery Cohort. * Ex Vivo Cohort will undergo placement of microdevice in the prostate after its surgical removal. * Surgery Cohort will undergo percutaneous placement of several microdevices in a selected tumor prior to surgery. This research study is a Pilot Study, which is the first-time investigators are examining this study intervention. The FDA (the U.S. Food and Drug Administration) has not approved the implantation of the microdevice for this specific disease, but usage of this has been approved for other uses.

Eligibility

Minimum Age: 22 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Brigham and Women's Hospital, Boston, Massachusetts, United States

Contact Details

Name: Adam S Kibel, MD

Affiliation: Brigham and Women's Hospital

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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