Trial Outcomes & Findings for MR Fingerprinting: A Novel Sequence Applied to Neuroimaging (NCT NCT03800537)

NCT ID: NCT03800537

Last Updated: 2023-06-12

Results Overview

Magnetic Resonance (MR) fingerprinting sequences will be examined to determine their utility for visualizing pathology.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

14 participants

Primary outcome timeframe

Immediately following MRI completion, within approximately 5 minutes

Results posted on

2023-06-12

Participant Flow

Participant milestones

Participant milestones
Measure
All Participants
All participants will receive the investigational MR Fingerprinting sequence. MR Fingerprinting: The MR fingerprinting technique requires less than 15 minutes and will be added following the standard MRI sequence.
Overall Study
STARTED
14
Overall Study
COMPLETED
10
Overall Study
NOT COMPLETED
4

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

MR Fingerprinting: A Novel Sequence Applied to Neuroimaging

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
All Participants
n=14 Participants
All participants will receive the investigational MR Fingerprinting sequence. MR Fingerprinting: The MR fingerprinting technique requires less than 15 minutes and will be added following the standard MRI sequence.
Age, Categorical
<=18 years
0 Participants
n=5 Participants
Age, Categorical
Between 18 and 65 years
12 Participants
n=5 Participants
Age, Categorical
>=65 years
2 Participants
n=5 Participants
Sex: Female, Male
Female
11 Participants
n=5 Participants
Sex: Female, Male
Male
3 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
14 Participants
n=5 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=5 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=5 Participants
Race (NIH/OMB)
Asian
0 Participants
n=5 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=5 Participants
Race (NIH/OMB)
Black or African American
4 Participants
n=5 Participants
Race (NIH/OMB)
White
10 Participants
n=5 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=5 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=5 Participants
Region of Enrollment
United States
14 Participants
n=5 Participants

PRIMARY outcome

Timeframe: Immediately following MRI completion, within approximately 5 minutes

Magnetic Resonance (MR) fingerprinting sequences will be examined to determine their utility for visualizing pathology.

Outcome measures

Outcome measures
Measure
All Participants
n=10 Participants
All participants will receive the investigational MR Fingerprinting sequence. MR Fingerprinting: The MR fingerprinting technique requires less than 15 minutes and will be added following the standard MRI sequence.
Percent of Participants With Visible Region of Interest (Imaging Visibility)
100 percentage of participants

Adverse Events

All Participants

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Desma Jones

University of North Carolina at Chapel Hill

Phone: 919-843-9463

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place