Clinical Trials Logo

Clinical Trial Summary

For the treatment for intermediate- and high-risk prostate cancer, Cyberknife boost will be used after 4 weeks of intensity modulated radiotherapy to pelvis. The boost doses are 18 Gy and 21 Gy in 3 fractions, respectively. The investigators plan to evaluate the toxicity of two dose groups and decide the appropriate dose for Cyberknife boost. Also, PSA control will be evaluated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03322020
Study type Interventional
Source Asan Medical Center
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 21, 2016
Completion date June 30, 2019

See also
  Status Clinical Trial Phase
Active, not recruiting NCT03344757 - Health Gatherings - For Your Health After Cancer N/A
Active, not recruiting NCT03149861 - Detection of Clinically Significant Prostate Cancer With 18F-DCFPyL PET/MR N/A
Not yet recruiting NCT05422911 - Abiraterone, Enzalutamide, or Apalutamide in Castrate-sensitive Prostate Cancer. Phase 2
Completed NCT01553188 - AMG 386 and Abiraterone for Advanced Prostate Cancer Phase 2
Completed NCT01819285 - Early Compared With Delayed Hormone Therapy in Treating Patients With Nonmetastatic Prostate Cancer Phase 3