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UnknownNCT04239599

Trial of Hypofractionated IMRT Boost Versus Conventional IMRT Boost for Localized High Risk Prostate Cancer

Randomized Trial of Concomitant Hypofractionated IMRT Boost Versus Conventional Fractionated IMRT Boost for Localized High Risk Prostate Cancer

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
178 (actual)
Sponsor
Sunnybrook Health Sciences Centre · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

Hypofractionation: 48 Gy in 25 fractions to pelvic lymph nodes while the prostate receives 68 Gy in 25 fractions concomitantly. Standard Fractionation: pelvic lymph nodes and prostate will initially be treated to 46 Gy in 23 fractions, followed by a subsequent boost to the prostate to a total dose of 78 Gy over 39 fractions.

Detailed description

Half the participants will receive using a one phase IMRT plan, the pelvic lymph nodes will be treated to a dose of 48 Gy in 25 fractions, while the prostate will be treated to a dose of 68 Gy in 25 fractions concomitantly (simulataneous integrated boost). The other half of the participants will receive Standard fractionation using 2 sequential IMRT plans, the pelvic lymph nodes and prostate will initially be treated to 46 Gy in 23 fractions, followed by a subsequent boost to the prostate to a total dose of 78 Gy.

Conditions

Interventions

TypeNameDescription
RADIATIONHypofractionated IMRT Radiation treatment

Timeline

Start date
2011-03-31
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2020-01-27
Last updated
2022-09-29

Source: ClinicalTrials.gov record NCT04239599. Inclusion in this directory is not an endorsement.

Trial of Hypofractionated IMRT Boost Versus Conventional IMRT Boost for Localized High Risk Prostate Cancer (NCT04239599) · Clinical Trials Directory