Data Collection for CAD Evaluation

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2012 by Universitaire Ziekenhuizen Leuven.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier:
NCT01600144
First received: May 14, 2012
Last updated: NA
Last verified: March 2012
History: No changes posted
  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:

Estimated Enrollment: 100
Study Start Date: March 2012
Groups/Cohorts Assigned Interventions
data collection Other: digital mammography
data collection

  Eligibility

Genders 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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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
  More Information

No publications provided

Responsible Party: Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier: NCT01600144     History of Changes
Other Study ID Numbers: s53792
Study First Received: May 14, 2012
Last Updated: May 14, 2012
Health Authority: Belgium: Institutional Review Board

Keywords provided by Universitaire Ziekenhuizen Leuven:
data mammography

ClinicalTrials.gov processed this record on July 20, 2014