- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01633866
Pediatric Radio Frequency Coils Generic
Pediatric Radio Frequency Coil Development on Clinical and Research MR Scanners
Study Overview
Status
Detailed Description
Pediatric Magnetic resonance (MR) imaging techniques have been limited by the unavailability of specialized radio-frequency (RF) coils for pediatric imaging. Typically, MR coils are designed for general purpose adult imaging and lack the mechanical design, flexibility and high channel count needed for pediatric imaging. Furthermore, pediatric patients are often positioned decubitus or prone rather than supine. This makes coil positioning even more challenging and often results in images with low SNR and poor image quality. Many coils used in clinical practice have fixed dimensions that do not fit within the realm of "one-size fits all," especially for the huge variation found in the pediatric patient population.
MRI coil development and optimization is performed by MR manufacturers and in research laboratories across the world including the Imaging Research Center (IRC) of Cincinnati Children's Hospital and Medical Center (CCHMC). Coil development and refinement involves evaluating the new coils on inert phantoms and then imaging examinations performed on healthy participants and patients. The focus of this study protocol is to evaluate the design and performance of investigational coils on patients and healthy participants.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Ohio
-
Cincinnati, Ohio, United States, 45229
- Cincinnati Children's
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Healthy participants:
- Male or Female
- Thermally stable
- Any age
Clinical patients:
- Male or Female
- Thermally stable
- any age
Exclusion Criteria:
Healthy participants & Clinical patients
- Female participants who are pregnant or lactating
- Subjects iwth standard contraindications to MRI
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Advances in Radio Frequency for MRI
advances in radio frequency (RF) coil magnetic resonance imaging (MRI)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of participants with adverse events as measured by heating and comfort participant response
Time Frame: Day 1
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
MRI Image Quality
Time Frame: 2 Weeks Post MRI Scan
|
2 Weeks Post MRI Scan
|
Collaborators and Investigators
Investigators
- Principal Investigator: Charles Dumoulin, PhD, Children's Hospital Medical Center, Cincinnati
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Musculoskeletal Diseases
- Nervous System Diseases
- Muscular Diseases
- Neuromuscular Diseases
- Genetic Diseases, Inborn
- Congenital Abnormalities
- Genetic Diseases, X-Linked
- Muscular Disorders, Atrophic
- Muscular Dystrophies
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Muscular Dystrophy, Duchenne
- Musculoskeletal Abnormalities
Other Study ID Numbers
- 2012-1041
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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