Case #18d: The study consists of healthful volunteers and compares temporal SNR attained which has a new fMRI pulse sequence with that from A different sequence. Does the study require human participants? Sure, the healthful volunteers are human contributors. Are classified as the individuals prospectively assigned to an intervention? No, in this c

Does the study entail human members? Sure Are definitely the contributors prospectively assigned to an intervention? No, not In this particular context. The transient stimulation of discomfort pathways along with the fMRI are being done to evaluate and describe brain activity, although not to switch it.   This study isn't a medical demo. NIDC

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