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Not Yet Recruiting NA INTERVENTIONAL NCT04809792

MR-Linac for Head and Neck SBRT

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

This study will evaluate the feasibility and safety of using MR-guided adaptive Head and Neck stereotactic radiotherapy (SBRT) at each fraction on the 1.5T MR-Linac.

Detailed Description

At the Sunnybrook Odette Cancer Centre (OCC), stereotactic body radiation therapy (SBRT) (35- 50 Gy in 5 fractions delivered 2x/week) has been employed in a subgroup of palliative Head and Neck cancer (HNC) patients, as part of an institutional protocol, when greater tumor response is desirable when compared to more palliative regimens. The MR-Linac has been approved by Health Canada for radiation treatment. With superior soft tissue contrast and the possibility for daily plan adaptation, it allows for higher treatment precision delivery, improved target coverage and greater normal tissue sparing. As a first step, this study will evaluate the feasibility and safety of using the 1.5T MR-Linac on patients with HNC who are treated with SBRT.

Interventions

Name: SBRT on the MR-Linac
Type: RADIATION
Description: Radiotherapy is performed on the 1.5 T MR Linac

Primary Outcomes

Measure: Proportion of patients who complete ≥80% of treatment fractions in ≤60 minutes.
TimeFrame: 2 years
Description: Clinical feasibility of delivering radiotherapy treatment on the MR Linac within 60 minutes and the need for patients to transfer to a CT-based linear accelerator will be monitored. The radiotherapy timing sheet will be used to record the length of time for patients to have their MR guided adaptive radiotherapy for each fraction.

Trial Information

NCT ID

NCT04809792

Status

Not Yet Recruiting

Study Type

INTERVENTIONAL

Phases

NA

Sponsor

Sunnybrook Health Sciences Centre

Last Updated

December 15, 2025