Single Fractions SBRT for Prostate Cancer
Recruiting now NCT04004312
Run by Fabio Cury · for 18 and older · Men
What this study is about
It is a phase I study of radical hypofractionation delivering one single fraction of SBRT in patients with low- and favorable intermediate-risk prostate cancer that will undergo placement of the SpaceOAR hydrogel prior to treatment. Our hypothesis is that treatments can be safely delivered in one single fraction using SBRT provided the separation between the prostate and rectum is increased using the hydrogel
Who can join (things the study team will check)
Inclusion Criteria: Histologically proven adenocarcinoma of the prostate. Tl-2b (AJCC 7th edition) Gleason score 6 or 7 (3+4)) or Gleason 7(4+3) and recent PSA \< 10 (less than 30 days; must obtained \>90 days from stopping dutasteride or \>30 days from stopping finasteride) Recent PSA under 15 ng/dL (less than 30 days; must obtained \>90 days from stopping dutasteride or \>30 days from stopping finasteride) OR Gleason 7(4+3) and recent PSA \< 10 (less than 30 days; must obtained \>90 days from stopping dutasteride or \>30 days from stopping finasteride) International Prostate Symptom Score \<16 Prostate gland volume\< 80cc Zubrod Performance Status 0-1 within 60 days prior to registration Age \>: 18 Patient must be able to provide study-specific informed consent prior to study entry. Exclusion Criteria: Patients who opt to receive another treatment modality, such as surgery, or undergo active surveillance. Prior or concurrent invasive malignancy (except non-melanomatous skin cancer) or lymphomatous/hematogenous malignancy unless continually disease free for a minimum of 5 years. All patients with in situ carcinoma are eligible for this study (for example, carcinoma in sit…
Where this trial is running
- McGill University Health Centre-Cedars Cancer Centre, Montreal, Quebec, Canada
Who to contact
Marianna Perna · 514-934-1934 · marianna.perna@muhc.mcgill.ca
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT04004312.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.