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Clinical Trial Summary

The purpose of this study is to determine the optimal radiation dose fractionation regimen for low grade follicular lymphoma. It is hypothesized that the complete response rate with the use of 12 Gy in 6 daily fractions is 80% (10% total width of the confidence interval) at 3 months. This phase II study will evaluate whether an intermediate dose for follicular lymphoma is associated with excellent response rates while minimizing acute and late toxicity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05284825
Study type Interventional
Source Sunnybrook Health Sciences Centre
Contact May Tsao, MD
Phone (416) 480-4806
Email may.tsao@sunnybrook.ca
Status Recruiting
Phase N/A
Start date February 28, 2022
Completion date January 1, 2025

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