Linear Source Registry for Prostate Cancer

  • End date
    Dec 24, 2022
  • participants needed
  • sponsor
    CivaTech Oncology
Updated on 24 January 2021


Ongoing follow up for subjects implanted with the Linear Source String for prostate cancer.


This registry is being conducted to provide long term analysis on the use of the linear Civastring source for prostate cancer. Prospective data collection will record and demonstrate biochemical response rates. Long term side effects and adverse events will be monitored.

Condition Malignant neoplasm of prostate, Prostatic disorder, Prostate Disorders, Prostate Cancer, Early, Recurrent, Prostate Cancer, prostate carcinoma, prostate cancers
Treatment Linear LDR Source
Clinical Study IdentifierNCT02516709
SponsorCivaTech Oncology
Last Modified on24 January 2021


Yes No Not Sure

Inclusion Criteria

Age > 18 years old
Plans to remain in care of enrolling physician for 5 years
> 5 years life expectancy
Signed informed consent
Enrolled within 6 weeks of implant or within 365 days of prior implant

Exclusion Criteria

Not willing or able to comply with protocol visit schedule
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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