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Adaptive CT Acquisition for Personalised Thoracic Imaging (ADAPT)

U

University of Sydney

Status

Completed

Conditions

Cancer, Lung

Treatments

Device: 4DCBCT images

Study type

Observational

Funder types

Other

Identifiers

NCT04070586
HREC/18/LPOOL/361

Details and patient eligibility

About

In this trial, Respiratory Motion Guided (RMG) 4DCBCT will be implemented for the first time on lung cancer patients. RMG-4DCBCT adapts the image acquisition as the patient's breathing changes (i.e. if the patient breathes faster, imaging data is acquired faster).

By adapting the acquisition to the dynamic patient, personalised images of a patients lungs are able to be acquired for radiotherapy treatments.

Full description

Four dimensional cone beam computed tomography (4DCBCT) continues to play a pivotal role in the safe delivery of radiotherapy treatments for lung cancer patients. 4DCBCT meets exacting tumour localisation requirements by allowing radiation therapists to measure the tumour as a patient breathes (4D=volumetric images plus respiratory induced tumour motion). Despite the success of 4DCBCT to date, it suffers from relatively poor image quality, very long scan times (4min) and higher imaging doses than are necessary. The primary reason for these problems is that although the purpose of 4DCBCT is to acquire information about tumour motion due to respiration, there is no feedback from the patients breathing signal to adapt and optimise the image acquisition process. This clinical trial is a phase 1 first in human's pilot study and the aim is therefore to prove feasibility of RMG-4DCBCT, not necessarily efficacy. As such, patient scans will be acquired across a broad range of patient breathing conditions to optimise the RMG-4DCBCT technique and also to plan a hypothesis driven clinical trial to follow.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have the ability to give informed consent
  • A diagnosis of lung cancer with an indication for radiotherapy either curative or palliative
  • Radiotherapy treatment involving the routine acquisition of CBCT for patient setup provided that 4DCBCT is to be acquired during the course of treatment.
  • At least two radiotherapy fractions during the course of treatment.

Exclusion criteria

  • Pregnant women.
  • Patient who in the opinion of the treating physician could not tolerate the extra time on the treatment couch for two days of treatment.

Trial design

30 participants in 1 patient group

4DCBCT images
Description:
4DCBCT images are acquired and assessed offline.
Treatment:
Device: 4DCBCT images

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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