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Breast Radiotherapy Audio Visual Enhancement for Sparing the Heart

NCT02881203 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2023-07-27

No results posted yet for this study

Summary

This study investigates the Breathe Well device to test whether it is superior to the existing treatment standard of the Varian Realtime Position Management (RPM) system in assisting patients with deep inspiration breath hold.

Conditions

Interventions

DEVICE

Breathe Well

Breathe Well is an audiovisual biofeedback device used to assist patients to regulate their breathing whilst undergoing radiation treatment.

DEVICE

RPM

Varian Real-time Position Management (RPM) system

Sponsors & Collaborators

  • University of Sydney

    lead OTHER

Principal Investigators

  • Gillian Lamoury, Medicine · Royal North Shore Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-15
Primary Completion
2021-09-30
Completion
2022-09-30

Countries

  • Australia

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02881203 on ClinicalTrials.gov