Evaluation of Technological Innovation in Radiotherapy

NCT03378856 · tracked via the Priya Life Science Canada tracker

Sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Phase

Observational

Started

2017-11-01

Last updated

2026-09-01

Condition(s) studied

CancerRadiotherapy Side Effect

Study summary

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.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Ability to provide informed consent * Receiving radiotherapy or brachytherapy Exclusion Criteria: \-

Primary outcome measure(s)

Accrual rates — 2 years
Determine feasibility of achieving high accural rates (greater than 80%) with this approach.

Trial sites (9)

Facility	City	Region	Status
BC Cancer - Kelowna	Kelowna	British Columbia	Recruiting
BC Cancer - Vancouver	Vancouver	British Columbia	Recruiting
London Health Regional Cancer Centre	London	Ontario	Recruiting
Sunnybrook Research Institute	Toronto	Ontario	Recruiting
Princess Margaret Cancer Centre	Toronto	Ontario	Recruiting
CISSS de Laval - Hôpital de la Cité-de-la-Santé	Laval	Quebec	Recruiting
Research Institute of the McGill University Health Center	Montreal	Quebec	Recruiting
Centre Hospitalier de l'Université de Montréal	Montreal	Quebec	Recruiting
CHU de Québec - Université Laval	Québec	Quebec	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03378856 on ClinicalTrials.gov ↗ ← All trials in Canada