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Clinical Trials/NCT01823094
NCT01823094
Completed
Not Applicable

CTP (Computed Tomography Perfusion) Imaging of Lung Cancer

University of California, Davis1 site in 1 country14 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non Small Cell Lung Cancer
Sponsor
University of California, Davis
Enrollment
14
Locations
1
Primary Endpoint
Yield of conducting CTP studies
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Investigators hope to learn more about how to use computed tomography (CT) scans to measure blood flow in lung tumors and how it may change in response to treatment. This measurement technique is called computed tomography perfusion (CTP). CT scanners use X-rays to produce 3-dimensional images of the body.

Currently, doctors determine the response to treatment by measuring the size of the tumor. Investigators are trying to find out if measuring the blood flow in the tumor is equal to or better than measuring the size of the tumor.

Detailed Description

This is an experimental study of CT perfusion (CTP) imaging in subjects with non-small cell lung cancer. The objectives of this study are to demonstrate the feasibility of CT blood flow measurements in lung cancer, to develop a foundation for the use of CT blood flow measurements in lung cancer to assess the response to treatment, and to develop an optimized CTP imaging protocol for evaluating blood flow in solid body tumors. In this study, tumor blood flow will be evaluated at baseline and follow-up routine CT examinations of patients with non-small cell lung cancer, and the response of tumor blood flow will be recorded as a secondary endpoint. This research study will entail two study visits - one required and one optional - which will coincide with regularly scheduled standard of care CT scans.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
June 2015
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • adult patients with non small cell lung cancer who receive, or are considered for, systemic therapy

Exclusion Criteria

  • renal failure pregnancy known contrast allergy

Outcomes

Primary Outcomes

Yield of conducting CTP studies

Time Frame: 2 years

Yield is determined as the percentage of assessable CTP studies, relative to all performed studies

Secondary Outcomes

  • Variability of CTP measurements(2 years)
  • Magnitude of treatment induced changes in tumor blood flow(2 years)

Study Sites (1)

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