Skip to content

Diagnostic Imaging of Bone Metastases in Prostate Cancer Patients

A Prospective Study Comparing the Diagnostic Accuracy of Bone SPECT-CT, Choline-PET-CT, PSMA-PET-CT, NaF-PET-CT and WB-MRI in the Detection of Prostate Cancer Bone Metastases

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03134261
Acronym
DIMAB
Enrollment
300
Registered
2017-04-28
Start date
2014-04-30
Completion date
2018-04-30
Last updated
2017-05-05

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

Conditions

Prostate Cancer Metastatic to Bone

Brief summary

An improved diagnosis of bone metastases in prostate cancer patients can have a significant impact on treatment strategy and probably survival as well. The primary purpose of the project is to determine the diagnostic accuracy of bone SPECT-CT, choline-PET-CT, PSMA-PET-CT, NaF-PET-CT and Whole-body MRI in the diagnosis of bone metastases in prostate cancer patients.

Detailed description

The project is a prospective diagnostic test accuracy study. The project takes place at Herlev Hospital and is a collaboration between the Department of Radiology and the Department of Clinical Physiology and Nuclear Medicine. The investigators want to include 300 prostate cancer patients referred to our standard diagnostic imaging (NaF-PET-CT scan) by the clinicians. In addition to the standard diagnostic imaging (NaF-PET-CT-scan), two project will be performed on all participants. The project has three arms with the following scanning combinations: A) Whole-body MRI + SPECT-CT B) Whole-body MRI + Cholin-PET-CT C) Whole-body MRI + PSMA-PET-CT The recruitment of project participants takes place on the day when the patients are undergoing a NaF-PET-CT scan in the course of regular clinical practice at our institution. All readers are experienced radiologists or specialists in nuclear medicine. Patient identification on each scan will be anonymized and the reader will not have access to clinical and biochemical information or previous imaging studies.

Interventions

DIAGNOSTIC_TESTWB-MRI

scanning methods

DIAGNOSTIC_TESTSPECT-CT

scanning methods

DIAGNOSTIC_TESTCholin-PET-CT

scanning methods

DIAGNOSTIC_TESTPSMA-PET-CT

Sponsors

Herlev Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Study participants will be allocated to the ongoing project arm at the time of enrollment.

Eligibility

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

Inclusion criteria

A subject will be eligible for project participation if he meets all of the following criteria: * Is either 1) a newly diagnosed prostate cancer patient in clinical suspicion of bone metastases or 2) a previously diagnosed prostate cancer patient in clinical suspicion of progression in the form of bone metastases. The subject must have been referred to the standard diagnostic imaging (18F-NaF-PET-CT) at our institution for bone metastases. * The prostate cancer diagnosis must be biopsy-proven * The subject is willing and able to comply with the protocol as judged by the investigator

Exclusion criteria

A subject will be excluded from the protocol if he meets one or more of the following criteria: * Has prior malignancy, except for adequately treated basal cell or squamous cell skin cancer * Has pacemaker or implanted devices (eg. cardiac valves, neurostimulator or insulin pump) that cannot be removed, metal clips/metal prostheses from surgery that are not MRI compatible or metallic foreign bodies in the eye (MRI

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracyThe two project scans will be performed within a maximum of 30 days from the performance of the NaF-PET-CT scanSensitivity and specificity

Countries

Denmark

Contacts

Primary ContactEva Dyrberg Mortensen, MD
eva.dyrberg@regionh.dk+45 38681002
Backup ContactHenrik S. Thomsen, Professor
henrik.thomsen@regionh.dk+45 38683212

Outcome results

None listed

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