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NCT03091816Completed

Dynamic Perfusion Computed Tomography in Patients With Localized Non-small Cell Lung Cancer

Dynamic Perfusion Computed Tomography Changes After Stereotactic Body Radiation Therapy for Localized Non-small Cell Lung Cancer

Source: ClinicalTrials.gov · Last updated 11 Jul 2024

Brief summary (registry, in English)

This pilot clinical trial studies the changes in dynamic perfusion computed tomography images before, during, and after stereotactic body radiation therapy in patients with stage I-II non-small cell lung cancer that has not spread to other parts of the body. Diagnostic imaging procedures, such as dynamic perfusion computed tomography, measure blood flow through tumors. Stereotactic body radiation therapy is a specialized radiation therapy that sends x-rays directly to the tumor using smaller doses over several days and may cause less damage to normal tissue. Giving dynamic perfusion computed tomography images before, during, and after stereotactic body radiation therapy may help better understand how radiation therapy works to stop tumor growth in patients with non-small cell lung cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
15 (actual)
First submitted
21 Mar 2017
Start date
8 May 2017
Primary completion date
2 Mar 2023
Lead sponsor
University of Southern California
Diseases
Lung cancer
NCT number
NCT03091816

What you commit to

  • Study type: Observational
  • Participants enrolled: 15
  • From 8 May 2017 to the primary completion date, 2 Mar 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients may not be receiving any other investigational agents

Other illness

  • Patients with nodal disease or distant metastatic disease
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • Patients with allergies to iodinated contrast not amenable to pre-medication

Other

  • Patients with tumors \< 1 cm
  • Patients must not be pregnant
  • Patients who are not able to lie supine with arms raised, and cooperate with breathholding instructions

Who the study is looking for

  • Biopsy proven non-small cell lung cancer
  • Minimum tumor dimension \>= 1 cm (preferably \>= 2 cm)
  • No clinical evidence of nodal disease (N1-N3) as assessed by CT and/or positron emission tomography (PET)/CT
  • Zubrod performance status 0-2
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
    • A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:
    • Has not undergone a hysterectomy or bilateral oophorectomy; or
    • Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)
  • No prior radiation to the same area
  • No concurrent chemotherapy
  • Evaluated by radiation oncologist to be appropriate SBRT candidate and scheduled to undergo SBRT as part of their care
  • Ability to understand and the willingness to sign a written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
USC / Norris Comprehensive Cancer Center
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.