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4D Imaging Techniques for Lung Cancer
N/A
Recruiting
Led By Daniel Saenz, PhD
Research Sponsored by The University of Texas Health Science Center at San Antonio
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients with cancer or presumed cancer involving the lung (primary or secondary) planned to undergo lung SBRT technique or IMRT technique with an SBRT setup in 10 or fewer fractions
Age ≥ 18 years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 weeks
Awards & highlights
Study Summary
This trial will compare two ways of taking CT scans to account for the fact that a patient's lungs move while receiving radiation therapy.
Who is the study for?
This trial is for adults over 18 with lung cancer (primary or secondary) who are set to undergo a specific type of radiation therapy in 10 or fewer sessions. They must be able to consent and understand English or Spanish. It's not suitable for those with poor lung function, multiple treatment targets at once, pregnant individuals, or anyone whose condition could affect therapy adherence.Check my eligibility
What is being tested?
The study compares two CT imaging techniques during radiation therapy for lung tumors: traditional free-breathing CT versus a more comprehensive CT that captures the entire breathing cycle. The goal is to see which method best aligns with patients' actual breathing during treatment.See study design
What are the potential side effects?
Since this trial focuses on imaging techniques rather than medication, typical drug side effects aren't expected. However, there may be discomfort from staying still during longer scans and potential risks associated with increased exposure to radiation.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am scheduled for a specific lung cancer radiation treatment in 10 or fewer sessions.
Select...
I am 18 years old or older.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
To investigate radiation therapy treatment tumor localization accuracy by determining whether the FB or AIP images is more representative of the target at treatment.
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: AIP (Average Intensity Projection) CT (Computed Tomagraphy)Active Control1 Intervention
An image taken over a longer time of the lungs (average intensity projection of 4DCT) will be compared with breathing during treatment.
Group II: FB (Free-Breathing) CTPlacebo Group1 Intervention
A snapshot of breathing (free-breathing traditional CT) will be used to compare with breathing during treatment.
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Who is running the clinical trial?
The University of Texas Health Science Center at San AntonioLead Sponsor
452 Previous Clinical Trials
91,365 Total Patients Enrolled
Daniel Saenz, PhDPrincipal InvestigatorUT Health San Antonio
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am scheduled for a specific lung cancer radiation treatment in 10 or fewer sessions.I am not currently pregnant.I am 18 years old or older.I am receiving treatment aimed at several cancer sites at once.My lung function is too poor for certain types of CT scans.
Research Study Groups:
This trial has the following groups:- Group 1: FB (Free-Breathing) CT
- Group 2: AIP (Average Intensity Projection) CT (Computed Tomagraphy)
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How many individuals have been included in this clinical experiment thus far?
"Affirmative. The evidence on clinicaltrials.gov verifies that this trial, which was initiated on August 17th 2021, is currently recruiting patients. 45 participants are sought from one research centre."
Answered by AI
Are there still vacancies for participation in this experiment?
"Clinicaltrials.gov indicates that the recruitment process for this medical trial is ongoing, with a commencement date of August 17th 2021 and an edit to the post on September 12th 2022."
Answered by AI
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