The objective of this study is to evaluate imaging quality and correlation with
histopathology in prostate cancer.
Device: MR imaging with endorectal coil
Device: MRI with endo-rectal coil
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Full eligibility criteria for NCT00930748
Ages eligible for Study
18 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
Age of patients: up to 80 years.
Men scheduled for radical prostatectomy due to prostate cancer or men post radical prostatectomy with suspicion of recurrence.
Patients who are able and willing to give consent and able to have an MRI examination.
Contraindications to MRI including: claustrophobia, weight over 120 kg, implanted ferromagnetic materials or foreign objects, and known intolerance to the MRI contrast agent (e.g. Gadolinium or Dotarem)
Individuals who are not able or willing to tolerate the required prolonged stationary supine position during imaging (approximately 1 hr.)
Any rectal pathology preventing probe insertion, (as active proctitis, active ulcerative colitis, fissure ani)
Any spinal pathology that prohibits maintaining supine position for an hour
Patients with documented myocardial infarction within one month of protocol entry, and patients with cardiac pacemakers
Severe cerebrovascular disease (multiple CVA or CVA within 6 months)
All locations for NCT00930748
Sheba Medical Center
Ramat Gan, Israel
View full eligibility
Tris trial is registered with FDA with number: NCT00930748. The sponsor of the trial is Sheba Medical Center and it is looking for 40 volunteers for the current phase.
Official trial title: Evaluation of the Potential of Endorectal MRI for the Staging and Recurrence of Prostate Cancer
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