Suspended

Use og Bone Scintigraphy, CT and MRI for Detection of Metastases in Patients With Breast Cancer

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Breast Diseases+3

+ Breast Neoplasms

+ Neoplasms

From 18 to 80 Years
+9 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: May 2008
See protocol details

Summary

Principal SponsorUniversity of Aarhus
Study ContactAnni Eskild-Jensen, MD, PhD, DMSci
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2008

Actual date on which the first participant was enrolled.

A new imaging modality combining CT and tomographic bone scintigraphy (SPECT/CT) has enabled the combination of functional and anatomical imaging. Its use in cancer patients has not yet been evaluated or validated against a relative gold stand or clinical follow up. The purposes of this study are: 1: to validate the use of conventional planar bone scintigraphy and SPECT combined with low-dose or diagnostic CT and compare this to 3 Tesla MRI and clinical follow up. 2: to compare the specificity of low-dose and diagnostic CT, respectively, combined with bone SPECT. 3: to construct an algorithm for optimal evaluation of disease dissemination in breast cancer patients

Official TitleUse og Bone Scintigraphy, CT and MRI for Detection of Metastases in Patients With Breast Cancer
NCT00682253
Principal SponsorUniversity of Aarhus
Study ContactAnni Eskild-Jensen, MD, PhD, DMSci
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

180 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 80 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Breast DiseasesBreast NeoplasmsNeoplasmsNeoplasms by SiteSkin DiseasesSkin and Connective Tissue Diseases

Criteria

4 inclusion criteria required to participate
Histological verified breast cancer

Age 18-80 years

Investigation for metastases using imaging modality/modalities planned

Written consent to participate in trial

5 exclusion criteria prevent from participating
Overweight limiting the use of MRI

Metal parts in body

Claustrophobia

Allergy to contrast agents used in trial

Show More Criteria

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Aarhus University Hospital

Aarhus, DenmarkOpen Aarhus University Hospital in Google Maps
SuspendedOne Study Center
Use og Bone Scintigraphy, CT and MRI for Detection of Metastases in Patients With Breast Cancer | PatLynk