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RECRUITING
NCT06794125
NA

An Evaluation of Dose-escalation for Intrathoracic Tumours

Sponsor: Chris Goodman

View on ClinicalTrials.gov

Summary

This is a pragmatic trial with patients randomized between standard of care palliative thoracic radiation therapy (RT) vs. hypofractionated, dose-escalated, esophageal-sparing (HD-ES) intensity modulated radiation therapy (IMRT). The investigators hypothesize that the use of advanced radiation planning techniques to optimize dose to esophagus will permit the safe delivery of a modestly dose-escalated five-fraction course of palliative radiation to intrathoracic malignancies. This approach aims to deliver higher biologically effective doses while improving toxicity when compared to conventional approaches with the goal of prolonging high-quality overall survival.

Official title: A Phase II/III Randomized Evaluation of Dose-escalation With Esophageal-sparing for Palliation of Intrathoracic Tumours (PREVENT)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

141

Start Date

2025-09-03

Completion Date

2029-03-01

Last Updated

2026-02-04

Healthy Volunteers

No

Conditions

Interventions

RADIATION

Hypofractionated Radiation Therapy

Hypofractionated, dose-escalated, esophageal-sparing intensity modulated radiation therapy

RADIATION

Radiation Therapy

standard of care palliative thoracic radiotherapy using volumetric modulated arc therapy/intensity-modulating radiotherapy

Locations (3)

British Columbia Cancer Agency Center for the Southern Interior

Kelowna, British Columbia, Canada

London Health Sciences Center Research Institute (Formerly Lawson Research Institute)

London, Ontario, Canada

Waterloo Regional Health Network

Waterloo, Ontario, Canada