Lesion Detection Assessment in the Liver: Standard vs Low Radiation Dose Using Varied Post-Processing Techniques
Status: | Recruiting |
---|---|
Conditions: | Colorectal Cancer, Cancer, Gastrointestinal |
Therapuetic Areas: | Gastroenterology, Oncology |
Healthy: | No |
Age Range: | 18 - 90 |
Updated: | 4/17/2018 |
Start Date: | May 9, 2017 |
End Date: | May 2021 |
Contact: | Corey T. Jensen, MD |
Email: | CR_Study_Registration@mdanderson.org |
Phone: | 713-745-3835 |
The goal of this clinical research study is to compare imaging software and 2 different
radiation doses during a standard CT scan in order to "see" problems in the liver and still
produce a good image quality.
This is an investigational study. The CT scans in this study are performed using an
FDA-approved and commercially available method. The comparison of software used in this study
at 2 different radiation doses is considered research.
Up to 104 participants will be enrolled in the study. All will take part at MD Anderson.
radiation doses during a standard CT scan in order to "see" problems in the liver and still
produce a good image quality.
This is an investigational study. The CT scans in this study are performed using an
FDA-approved and commercially available method. The comparison of software used in this study
at 2 different radiation doses is considered research.
Up to 104 participants will be enrolled in the study. All will take part at MD Anderson.
If you agree to take part in this study, you will have a CT scan that is done as part of your
routine care. This CT scan will be done at the normal radiation dose.
During this scan, you will also have a scan of the liver at a lower radiation dose, which is
part of the research in this study. This will add about a minute to your normal scan time.
Information will also be collected from your medical record.
After your scan, your participation in this study will be over.
routine care. This CT scan will be done at the normal radiation dose.
During this scan, you will also have a scan of the liver at a lower radiation dose, which is
part of the research in this study. This will add about a minute to your normal scan time.
Information will also be collected from your medical record.
After your scan, your participation in this study will be over.
Inclusion Criteria:
1. Patient must be >/= 18 years of age and =90 years of age
2. Men and non-pregnant women
3. Pathology proven diagnosis of colon or colorectal carcinoma
4. Liver metastases on most recent prior M.D. Anderson CT examination
5. Standard of care CT abdomen examination planned WITH IV contrast
Exclusion Criteria:
1. Patients cannot give informed consent
2. Patients cannot undergo CT examination
We found this trial at
1
site
1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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