Body Magnetic Resonance (MR) Imaging Techniques
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Johns Hopkins University
- Enrollment
- 36
- Locations
- 1
- Primary Endpoint
- Magnetic resonance signal
Study Overview
Brief Summary
Any patient already receiving a scheduled MR scan of the body for any clinical indication will be eligible for this program.
Detailed Description
If patients agree to participate in this program, it would require only a slightly longer examination time. This time would vary according to the body area/organ being visualized but would not exceed 30 minutes over the length of the clinical examination. Volunteers are eligible if they are willing to undergo an MR examination.
Patients would not be required to make any additional visits beyond their clinically-indicated visits. The study duration would vary according to the body area/organ visualized but would not exceed 30 minutes over the length of the clinical examination. Volunteers would be required to keep one study appointment to include one MR imaging examination.
There will be no interruption to the standard care given to patients who participate in this trial since the clinical portion of their examination will be completed prior to the study portion of the exam.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- — to 100 Years (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Male or Female clinically scheduled to undergo MR Imaging at Johns Hopkins Medical Institutions
Exclusion Criteria
- •Contraindications to MR Imaging
Outcomes
Primary Outcomes
Magnetic resonance signal
Time Frame: One Hour
Magnetic resonance imaging acquires signal from the human body. The signal will be measured at the time of the patient study. The amount of signal change will be measured between subjects.
Secondary Outcomes
No secondary outcomes reported