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Pilot Investigation of Dual Energy CT Imaging on an Online Adaptive Radiation Therapy System

Pilot Investigation of Dual Energy CT Imaging on an Online Adaptive Radiation Therapy System

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07219134
Enrollment
30
Registered
2025-10-21
Start date
2025-06-06
Completion date
2026-04-08
Last updated
2026-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Genitourinary System Carcinoma, Malignant Pelvic Neoplasm

Brief summary

This study is being done to see if researchers can find a better way to image a patient's tumor during radiation treatment.

Interventions

OTHERNon-Interventional Study

Non-interventional study

Sponsors

University of Michigan Rogel Cancer Center
Lead SponsorOTHER
Varian Medical Systems, Inc.
CollaboratorUNKNOWN

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \* Patients with pelvis or genitourinary (GU) cancer requiring standard of care radiotherapy treatment * All adults, defined as individuals of 18 years of age or greater * Radiotherapy treatment will be performed on the Varian Ethos radiotherapy system * Ability to understand and the willingness to sign a written informed consent

Exclusion criteria

* \* Minors, defined as individuals less than 18 years of age * Pregnant or nursing female

Design outcomes

Primary

MeasureTime frameDescription
Image quality- MeanUp to 2 yearsThe primary analysis will compare imaging quality endpoints processed by DE-CBCT and the standard of care SE-CBCT, with the latter representing the standard clinical acquisition. Descriptive statistics will be computed for the image quality metrics from each imaging modality and for the difference in metrics between the modalities. A paired t-test or Wilcoxon signed-rank test will compare the distribution of the image quality metrics between DE-CBCT and standard of care SE-CBCT. Secondary analysis will compare image quality endpoints between DE-CBCT and standard of care conventional planning CT.
Image quality- medianUp to 2 yearsThe primary analysis will compare imaging quality endpoints processed by DE-CBCT and the standard of care SE-CBCT, with the latter representing the standard clinical acquisition. Descriptive statistics will be computed for the image quality metrics from each imaging modality and for the difference in metrics between the modalities. A paired t-test or Wilcoxon signed-rank test will compare the distribution of the image quality metrics between DE-CBCT and standard of care SE-CBCT. Secondary analysis will compare image quality endpoints between DE-CBCT and standard of care conventional planning CT.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRobert Dess

University of Michigan Rogel Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026