[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100615357":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":29,"locations":35,"responsibleParty":49,"collaborators":51,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":25,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":61,"maxAge":25,"enrollmentInfo":62,"targetDuration":25,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":71,"overallStatus":74,"whyStopped":25,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},{"fullName":5,"class":6},"AHS Cancer Control Alberta","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Prostate Only Radiation Therapy (PORT)","ACTIVE_COMPARATOR","Radiation therapy: prostate and surrounding tissues",[13],"Radiation: Prostate Only Radiation Therapy (PORT)",{"label":15,"type":16,"description":17,"interventionNames":18},"Prostate + Whole Pelvis Radiation Therapy (P-WPRT)","EXPERIMENTAL","Radiation therapy: prostate and surrounding tissues + whole pelvis radiation therapy",[19],"Radiation: Prostate + Whole Pelvis Radiation Therapy (P-WPRT)",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"RADIATION","6800cGy in 25 daily fractions to the prostate and surrounding tissues",[9],null,{"type":22,"name":15,"description":27,"armGroupLabels":28,"otherNames":25},"6800cGy to the prostate and surrounding tissues + 5000cGy to the whole pelvis in 25 daily fractions.",[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"Lindsay Rowe, MD","CONTACT","780-432-8966","Lindsay.rowe@ahs.ca",[36],{"facility":37,"status":25,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":25},"Cross Cancer Institute","Edmonton","Alberta","T6G 1Z2","Canada","CA",{"type":44,"coordinates":45},"Point",[46,47],-113.46871,53.55014,{"lat":47,"lon":46},{"type":50,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR",[52],{"name":37,"class":6},"100615357","phase-2-psma-pet-directed-radiation-therapy-for-high-risk-prostate-cancer-100615357",false,"NCT07291557","PSMA-PET Directed Radiation Therapy for High-Risk Prostate Cancer","PSMA-PET Directed Radiation Therapy in High and Very High-Risk Prostate Cancer","Inclusion Criteria:\n\nPSMA-N0M0 patients who have a documented history of High Risk localized adenocarcinoma of the prostate are eligible to participate if they meet the following eligibility criteria:\n\n1. Participants capable of giving written informed consent.\n2. Male.\n3. Age ≥18 years.\n4. ECOG ≤2.\n5. Patient has histologically proven adenocarcinoma of prostate gland with an assigned Gleason score and Gleason Grade Group.\n6. ≥NCCN High-Risk localized disease as per standard imaging investigations including pelvic imaging (CT, MRI) and 99Tc bone scan. High Risk prostate cancer defined as any of the following: cT3-T4 disease OR PSA ≥20 ng\u002Fml OR Gleason grade group 4 or 5.\n7. No documentation of regional nodal (N1) or metastatic (M1) prostate cancer on standard imaging (CT, MRI, or 99Tc bone scan).\n8. In the opinion of the treating oncologist, patient is fit to undergo radical external beam radiotherapy to the prostate.\n9. Patient commits to androgen suppression treatment as per standard of care. 10. Patient is willing to complete symptom and patient reported outcome questionnaires.\n\n11\\. Patients of childbearing \u002F reproductive potential should use highly effective birth control methods, as defined by the investigator, during the study treatment period and for a period of 6 months after the last dose of radiation therapy. A highly effective method of birth control is defined as those that result in low failure rate (i.e. less than 1% per year) when used consistently and correctly. Note: abstinence is acceptable if this is established and preferred contraception for the patient and is accepted as a local standard.\n\nMale patients should agree to not donate sperm during the study and for 6 months after completion of radiation therapy.\n\nExclusion Criteria:\n\n1. Inability to complete the investigational imaging examinations due to other reasons (severe claustrophobia, radiation phobia, etc.).\n2. Any additional medical condition, serious inter-current illness or other extenuating circumstance that, in the opinion of the Investigator, may significantly interfere with study performance, interpretation, or compliance with radiation\n3. Patients who have initiated therapy (ADT, systemic therapy, or radiation) for their prostate cancer prior to PSMA-PET imaging.\n4. History of inflammatory bowel disease, anal stenosis, colorectal surgery, or repeated endoscopic examinations\u002Finterventions related to anorectal diseases.\n5. History of prostatectomy or previous pelvic radiotherapy.\n6. Previous malignancy within the last five years, except BCC or SCC skin or a malignancy treated curatively with no evidence of disease for ≥5 years.\n7. Bilateral hip prostheses will be ineligible for study","MALE","18 Years",{"count":63,"type":64},250,"ESTIMATED","INTERVENTIONAL",[67],"PHASE2","In this study, prostate cancer patients whose cancer has not spread to the lymph nodes will receive radiation therapy targeted to the prostate and nearby tissues with or without whole pelvis radiation therapy. PSMA imaging will be used to visualize prostate cancer prior to starting the trial.",[70],"Prostate Cancer",[72,73],"Radiotherapy","PSMA","NOT_YET_RECRUITING","2025-12-05",{"date":77,"type":78},"2025-12-18","ACTUAL",{"date":80,"type":64},"2026-05",{"date":82,"type":64},"2036-05",{"name":5,"class":6},1]