Back to search results
NCT02091518

Development and Evaluation of Magnetic Resonance Imaging Acquisition and Analysis Methods

Enrolling by Invitation
NAAges 18+InterventionalDiagnostic
Memorial Sloan Kettering Cancer Center
~672 participants
Updated 2026-08-17 on ClinicalTrials.gov
What's tested:MR Screening QuestionnaireMagnetic Resonance Imaging Acquisition and Analysis

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
feasibility of new MRI applications
Measured over 5 years

Conditions

Healthy

Explore related trials

Healthy VolunteersPatients

NCT02091518

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Memorial Sloan Kettering Cancer Center

    New York, New Yorkno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Oguz Akin, MD · PRINCIPAL_INVESTIGATOR · Memorial Sloan Kettering Cancer Center

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Men and women age 18 or older

Exclusion

Anyone who would be normally excluded from undergoing an MRI examination as per Memorial Hospital for Cancer and Allied Diseases Screening Questionnaire for MRI
Patients/volunteers with a pacemaker, aneurysm clip or any other condition that would warrant avoidance of a strong magnetic field
Female patients/ volunteers who are pregnant or nursing
Patients/ volunteers who are unable to comply or complete the MRI exam due to claustrophobia or high levels of anxiety
Patients/ volunteers from the vulnerable population, as defined by 45 CFR 46.
Patients at higher risk due to age, frailty, or the emergent nature of their condition

What this trial measures

  • feasibility of new MRI applications5 years

    This protocol will provide pilot data to determine the feasibility of development and optimization of new MRI acquisition and analysis method.including sequence development, optimization, and workflow and analysis/visualization tools. An investigator will view the conventional images, as well as the additional research sequences. The radiologist will then complete data forms for each image and quantitative values, as listed in the evaluation form will be recorded. After all images have been read, the radiologist will review the clinical images together with the research images, and determine whether the research sequences had any effect on their diagnostic confidence.