Disposable Perfusion Phantom for Accurate DCE (Dynamic Contrast Enhanced)-MRI Measurement of Pancreatic Cancer Therapy Response

The University of Alabama at Birmingham

Status

Enrolling

Conditions

Pancreatic Cancer

Treatments

Device: Point-of-care Portable Perfusion Phantom, P4

Study type

Interventional

Funder types

Other

Identifiers

NCT04588025

IRB- 300003007

Details and patient eligibility

About

The goal of this study is to investigate whether the therapeutic response of pancreatic tumors can be accurately assessed using quantitative DCE-MRI, when the inter/intra-scanner variability is reduced using the Point-of-care Portable Perfusion Phantom, P4. The intra-scanner variability over time leads to errors in therapy monitoring, while the inter-scanner variability impedes the comparison of data among institutes. The P4 is small enough to be imaged concurrently in the bore of a standard MRI scanner with a patient for real-time quality assurance. The P4 is safe, inexpensive and easily operable, thus it has great potential for widespread and routine clinical use for accurate diagnosis, prognosis and therapy monitoring.

This study has identified two arms, one arm is healthy individuals that will undergo DCE MRI at three different MRI locations to establish baseline results. The healthy volunteers will undergo these MRIs prior to the second arm, which contains patients with pancreatic cancer. The pancreatic cancer patients will only have DCE MRI done at one location.

Enrollment

55 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Healthy Volunteer - a small number of healthy volunteers (5) will be used as the control group.

Inclusion Criteria:

Targeted/planned enrollment in the study will include all racial/ethnic groups with no groups excluded on the basis of race, ethnicity or gender.
Participants should be 19 years of age or older
Participants should not have any known major health problems including but not limited to cancers, heart diseases, diabetes, high blood pressure and/or cholesterol, stroke, respiratory problems, and arthritis.

Exclusion Criteria:

Participants having any known major health problems will be excluded.
Participants with safety contraindications to MRI examination (determined by standard clinical screening).
Participants on hemodialysis or with acute renal failure will be excluded. (Participants on hemodialysis and those with renal failure who receive intravenous gadolinium may be at increased risk for a condition called Nephrogenic systemic fibrosis/ Nephrogenic fibrosing dystrophy and thus will be excluded.)
Participants may not be pregnant or lactating.
Participants may not father a child while on this study as the treatment may indirectly affect an unborn child.
Unless participants cannot have children because of surgery or other medical reasons, participants must have been using an effective form of birth control before starting the study.
Participants must also agree to continue to use an effective form of birth control for 6 months after taking the study. Effective birth control includes birth control pills, patch, IUD (intrauterine device), condom, sponge, diaphragm with spermicide, or avoiding sexual activity that could cause pregnancy.

Pancreatic Cancer Participants:

Inclusion Criteria:

Patients having biopsy proven locally advanced pancreatic cancer will be asked to participate in this study.
Targeted/planned enrollment in the study will include all racial/ethnic groups, with no groups excluded on the basis of race, ethnicity or gender.
Participants should be 19 years of age or older.

Exclusion Criteria:

Participants with safety contraindications to MRI examination (determined by standard clinical screening).
Participants on hemodialysis or with acute renal failure will be excluded.
Participants on hemodialysis and those with renal failure who receive intravenous gadolinium may be at increased risk for a condition called Nephrogenic systemic fibrosis/ Nephrogenic fibrosing dystrophy and thus will be excluded.
Participants may not be pregnant or lactating.
Participants may not father a child while on this study as the treatment may indirectly affect an unborn child.
Unless participants cannot have children because of surgery or other medical reasons, participants must have been using an effective form of birth control before starting the study.
Participants must also agree to continue to use an effective form of birth control for 6 months after taking the study. Effective birth control includes birth control pills, patch, IUD, condom, sponge, diaphragm with spermicide, or avoiding sexual activity that could cause pregnancy.