Evaluation of Technological Innovation in Radiotherapy

Recruiting now

Conditions studied: Cancer, Radiotherapy Side Effect

In brief

Prospective cohort study of patients receiving standard-care radiotherapy is paramount to a better understanding of radiation effects and longterm outcomes. The primary objective is to determine the feasibility of establishing infrastructure to systematically collect clinical data, patient-reported outcomes, and imaging data from daily radiotherapy practice. Secondary objectives are to provide a control cohort for comparative effectiveness research of investigational interventions through a cmRCT design; compare imaging features with clinical outcomes; understand dose-effect relationships; quantify imaging quality metrics.

Key facts

Study ID

NCT03378856

Run by

Centre hospitalier de l'Université de Montréal (CHUM)

People needed

1500

Starts

2017-11-01

Expected to finish

2025-10-01

Last updated by the study team

2024-12-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ability to provide informed consent
• Receiving radiotherapy or brachytherapy

Where it is running

• Centre de santé et de services sociaux de Laval — Laval, Quebec, Canada (enrolling)
• Centre Hospitalier de l'Université de Montréal — Montreal, Quebec, Canada (enrolling)
• London Health Regional Cancer Centre — London, Ontario, Canada
• Princess Margaret Cancer Centre — Toronto, Ontario, Canada
• CHUQ — Québec, Quebec, Canada

Full record on ClinicalTrials.gov

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