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NCT03424850
Safety and Efficacy of 21 Gy, 23 Gy and 25 Gy for High Dose Rate (HDR) Prostate Brachytherapy
The purpose of this research study is to learn more about the outcomes and early and late side effects of treating early stage prostate cancer with high dose rate brachytherapy.
Trial Details
NCT ID NCT03424850
Phase PHASE1 / PHASE2
Sponsor Washington University School of Medicine
Status RECRUITING
Cancer Type Prostate Cancer
Interventions
Locations (sample) St Louis, Missouri, United States|38.62727,-90.19789
Key Eligibility Criteria
Histologically or cytologically confirmed diagnosis of early stage prostate cancer. Must be considered either low-risk (T1-T2a, Gleason ≤ 6, PSA \< 10 ng/mL) or favorable intermediate-risk (Gleason 3 +4 = 7, percentage of positive … Prior androgen deprivation therapy is allowed and may have been initiated up to 6 months prior to the date of the HDR implant. The complete duratio… At least 18 years of age.
For full eligibility, visit ClinicalTrials.gov .
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