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PCMRI - an MRI/TRUS System for the Evaluation of the Prostate

NCT00542100 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2007-10-10

No results posted yet for this study

Summary

The aim of the clinical study is to evaluate the convenience and efficacy of the PCMRI in the assessment of the prostate in humans.

The study cohort will include 50 patients and is designed to be non-comparative to other diagnostic methods.

Conditions

Interventions

DEVICE

PCMRI

Sponsors & Collaborators

  • TopSpin Medical

    lead INDUSTRY

Principal Investigators

  • Shmuel Cytron, MD. · Barzilai Medical Center, Ashkelon, Israel

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
80 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-11-30
Completion
2008-11-30

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00542100 on ClinicalTrials.gov