The Value of Advanced MR Imaging in Gynecological Tumors and Benign Uterine Fibroids (NCT03993210) | Clinical Trial Compass
TerminatedNot Applicable
The Value of Advanced MR Imaging in Gynecological Tumors and Benign Uterine Fibroids
Stopped: Key personnel moving out
United States1 participantsStarted 2019-09-18
Plain-language summary
This research is being done to test new MRI methods called Magnetic Resonance Fingerprinting and Q-space Trajectory Imaging in gynecological abnormalities. The purpose of this research study is to evaluate if these new MRI methods can give additional information in characterizing gynecological tumors compared with conventional MRI.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participants with suspected or histologically confirmed diagnosis of primary or recurrent gynecological cancer including uterine endometrial, cervical, vaginal, vulvar, ovarian, and smooth-muscle tumors undergoing routine clinical standard of care pelvic MRI
* Control subjects with benign fibroids undergoing routine clinical standard of care pelvic MRI
* Age ≥ 18 years
* ECOG performance status of ≤ 2, based on treating physician's discretion (Appendix A)
* Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
* Contraindication to MRI identified by the MR procedure screening form, such as a pacemaker, aneurysm clip, inner ear implant, neurostimulator, or other MR non-compatible device or implant
* Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
* Adults unable to consent
* Non-english speaking subjects
* Pregnant women
* Prisoners