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Data Collection for CAD Evaluation

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2012 by Universitaire Ziekenhuizen Leuven.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01600144
First Posted: May 16, 2012
Last Update Posted: August 7, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Universitaire Ziekenhuizen Leuven
  Purpose
Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.

Condition Intervention
Data Collection Other: digital mammography

Study Type: Observational
Study Design: Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Universitaire Ziekenhuizen Leuven:

Primary Outcome Measures:
  • Datacollection [ Time Frame: 2 years ]
    No outcome described, only datacollection


Estimated Enrollment: 100
Study Start Date: March 2012
Estimated Primary Completion Date: August 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
data collection Other: digital mammography
data collection

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
women
Criteria

Inclusion Criteria:

  • women who underwent a digital mammography imaging

Exclusion Criteria:

  • men
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01600144


Contacts
Contact: Chantal Van Ongeval, MD,Phd (0)16343746 ext +32 chantal.vanongeval@uzleuven.be

Locations
Belgium
UZLeuven Recruiting
Leuven, Belgium, 3000
Contact: Hilde Vandenhoutte, PhD    (0)16343636 ext 32    hilde.vandenhoutte@uzleuven.be   
Principal Investigator: Chantal Van Ongeval, MD,Phd         
Sponsors and Collaborators
Universitaire Ziekenhuizen Leuven
Investigators
Principal Investigator: Chantal Van Ongeval, MR,Phd Universitaire Ziekenhuizen Leuven
  More Information

Responsible Party: Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier: NCT01600144     History of Changes
Other Study ID Numbers: s53792
First Submitted: May 14, 2012
First Posted: May 16, 2012
Last Update Posted: August 7, 2014
Last Verified: March 2012

Keywords provided by Universitaire Ziekenhuizen Leuven:
data mammography