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Evaluation of MRI for Prostate Cancer

Evaluation of the Potential of Endorectal MRI for the Staging and Recurrence of Prostate Cancer

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00930748
Enrollment
40
Registered
2009-06-30
Start date
2008-11-30
Completion date
2011-06-30
Last updated
2011-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostatic Neoplasms

Brief summary

The objective of this study is to evaluate imaging quality and correlation with histopathology in prostate cancer.

Detailed description

The objective of this study is to evaluate of the potential of endorectal 3T MRI for the staging of prostate cancer before prostatectomy or recurrence of prostate cancer after prostatectomy

Interventions

DEVICEMR imaging with endorectal coil

MR imaging with endorectal coil

DEVICEMRI with endo-rectal coil

MRI with endo-rectal coil

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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)

Design outcomes

Primary

MeasureTime frame
• MRI and pathology correlation2 years

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026