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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04643015
Other study ID # 20-482
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 18, 2020
Est. completion date November 18, 2025

Study information

Verified date December 2023
Source Memorial Sloan Kettering Cancer Center
Contact Gerald Behr, MD
Phone 212-639-6470
Email behrg@mskcc.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is being done to see how we can prevent problems caused by movement during the MRI scan. Different ways of doing the scan (techniques) will be tested to see if they are practical and can prevent problems related to motion. For example, changes in the timing of the magnetic field and the radio waves will be examined, and at changes in the way a computer is used to process the images. The new techniques will be compared with the techniques that are usually used.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date November 18, 2025
Est. primary completion date November 18, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients of any age, including males and females, who are being treated in the Department of Pediatrics and are already scheduled to undergo MRI Exclusion Criteria: - Anyone who would normally be excluded from undergoing an MRI examination as per Memorial Hospital for Cancer and Allied Diseases Screening Questionnaire for MRI (Appendix A). Subjects with pacemakers or aneurysm clips that are MRI conditional or MRI compatible may enroll in the study if the study is clinically indicated. - Female patients who are pregnant - Patients who are unable to comply or complete the MRI exam due to claustrophobia or high levels of anxiety - Patients at higher risk due to age, frailty, or the emergent nature of their condition - Patients who are undergoing MRI only of the head, neck or spine

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
MRI
Briefly, new MRI sequences will be used on a patient who is undergoing a scheduled, clinically necessary MRI exam. Any new research sequence will be scanned in addition to the clinically required sequences and will not interfere with the clinical scan other than requiring five to ten minutes of additional "table time". There will be no invasive measures under this protocol.

Locations

Country Name City State
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compare Image Quality To assess the new MRI sequences or MRI analysis methods and compare their image quality to current clinical ones. Specifically, we aim to compare the routine sequences with the experimental sequences. Day of MRI
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