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RECRUITING
NCT06331013
NA

CyberKnife Ultra-hypofractionated SBRT for Localized PROStatE cancEr

Sponsor: European Institute of Oncology

View on ClinicalTrials.gov

Summary

This is a prospective observational study. The study will proceed with the enrollment of 60 patients in 2 years. he aim of the present study is to evaluate effectiveness of ultra-hypofractionated (UH) CyberKnife Stereotactic Body Radiation Therapy treatment on the whole prostate gland plus Simultaneous integrated boost (SIB) to the dominant intraprostatic lesions (DIL(s) in intermediate-unfavourable to high-risk Prostate Cancer (PCa) patients.

Official title: CyberKnife Ultra-hypofractionated SBRT for Localized PROStatE cancEr With Dose-escalation to the Dominant Intraprostatic Lesion: is the Juice Worth the Squeeze? The PRO-SPEED Trial

Key Details

Gender

MALE

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2023-02-20

Completion Date

2029-12-31

Last Updated

2025-08-28

Healthy Volunteers

No

Conditions

Interventions

RADIATION

CyberKnife ultra-hypofractionated SBRT

CyberKnife ultra-hypofractionated SBRT for localized Prostate cancer with dose-escalation to the dominant intraprostatic lesion

Locations (1)

European Institute of Oncology

Milan, Italy