- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01600144
Data Collection for CAD Evaluation
August 6, 2014 updated by: Universitaire Ziekenhuizen KU Leuven
Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Chantal Van Ongeval, MD,Phd
- Phone Number: +32 (0)16343746
- Email: chantal.vanongeval@uzleuven.be
Study Locations
-
-
-
Leuven, Belgium, 3000
- Recruiting
- UZLeuven
-
Principal Investigator:
- Chantal Van Ongeval, MD,Phd
-
Contact:
- Hilde Vandenhoutte, PhD
- Phone Number: 32 (0)16343636
- Email: hilde.vandenhoutte@uzleuven.be
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
women
Description
Inclusion Criteria:
- women who underwent a digital mammography imaging
Exclusion Criteria:
- men
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
data collection
|
data collection
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Datacollection
Time Frame: 2 years
|
No outcome described, only datacollection
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Chantal Van Ongeval, MR,Phd, Universitaire Ziekenhuizen KU Leuven
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2012
Primary Completion
August 1, 2014
Study Registration Dates
First Submitted
May 14, 2012
First Submitted That Met QC Criteria
May 14, 2012
First Posted (Estimate)
May 16, 2012
Study Record Updates
Last Update Posted (Estimate)
August 7, 2014
Last Update Submitted That Met QC Criteria
August 6, 2014
Last Verified
March 1, 2012
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- s53792
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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