SBRT vs. Conventional Fractionation With HDR Boost for Prostate Cancer
Recruiting now · Not applicable
Conditions studied: Prostate Cancer
In brief
Random assignment between SBRT and conventionally fractionated boost following HDR brachytherapy for prostate cancer.
Key facts
- Study ID
- NCT04861415
- Run by
- Dr. Gerard Morton
- People needed
- 55
- Starts
- 2020-12-23
- Expected to finish
- 2027-12-23
- Last updated by the study team
- 2023-04-12
Who can join
Age: 18 and older. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- Age 18 or older
- Informed consent for treatment and study participation completed
- Pathologically proven diagnosis of prostate adenocarcinoma
- ECOG Performance Status 0-2
- No prior history of pelvic radiotherapy, brachytherapy, cryosurgery, HIFU, TURP or radical prostatectomy
You may not qualify if…
- Presence of nodal or distant metastasis on staging MRI or CT Abdomen/Pelvis and Bone scan within 90 days of enrolment (CT/MRI/Bone Scan are only required if the clinical risk of metastatic disease is sufficient to warrant these scans)
- Plan for adjuvant chemotherapy post-radiotherapy
- Serious medical comorbidities or other contraindications to HDR brachytherapy
- Presence of inflammatory bowel disease
- Presence of connective tissue disorder seen as a contraindication to radiotherapy
- Medically unfit for general/spinal anesthesia
- Unable or unwilling to complete questionnaires
Where it is running
- Sunnybrook Health Sciences Centre — Toronto, Ontario, Canada (enrolling)
Full record on ClinicalTrials.gov
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